Canonical Allele Identifier: CA386304035
Gene: PAH HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.103288568C>G (hg19) chr12:g.102894790C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102894790C>G , CM000674.2:g.102894790C>G GRCh38
NC_000012.11:g.103288568C>G , CM000674.1:g.103288568C>G GRCh37
NC_000012.10:g.101812698C>G NCBI36
NG_008690.1:g.27813G>C
NG_008690.2:g.68621G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.297G>C MANE Select ENSP00000448059.1:p.Arg99Ser
ENST00000307000.7:c.282G>C ENSP00000303500.2:p.Arg94Ser
ENST00000546844.1:c.297G>C ENSP00000446658.1:p.Arg99Ser
ENST00000548928.1:n.219G>C
ENST00000549111.5:n.393G>C
ENST00000550978.6:c.281G>C
ENST00000551337.5:c.297G>C ENSP00000447620.1:p.Arg99Ser
ENST00000551988.5:n.386G>C
ENST00000553106.5:c.297G>C ENSP00000448059.1:p.Arg99Ser
NM_000277.1:c.297G>C NP_000268.1:p.Arg99Ser
XM_011538422.1:c.297G>C XP_011536724.1:p.Arg99Ser
NM_000277.2:c.297G>C NP_000268.1:p.Arg99Ser
NM_001354304.1:c.297G>C NP_001341233.1:p.Arg99Ser
XM_017019370.2:c.297G>C XP_016874859.1:p.Arg99Ser
NM_000277.3:c.297G>C MANE Select NP_000268.1:p.Arg99Ser
NM_001354304.2:c.297G>C NP_001341233.1:p.Arg99Ser
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