Canonical Allele Identifier: CA386297029
Gene: PAH HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.103249099A>C (hg19) chr12:g.102855321A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102855321A>C , CM000674.2:g.102855321A>C GRCh38
NC_000012.11:g.103249099A>C , CM000674.1:g.103249099A>C GRCh37
NC_000012.10:g.101773229A>C NCBI36
NG_008690.1:g.67282T>G
NG_008690.2:g.108090T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.521T>G MANE Select ENSP00000448059.1:p.Ile174Ser
ENST00000307000.7:c.506T>G ENSP00000303500.2:p.Ile169Ser
ENST00000549111.5:n.617T>G
ENST00000551988.5:n.542T>G
ENST00000553106.5:c.521T>G ENSP00000448059.1:p.Ile174Ser
NM_000277.1:c.521T>G NP_000268.1:p.Ile174Ser
XM_011538422.1:c.521T>G XP_011536724.1:p.Ile174Ser
NM_000277.2:c.521T>G NP_000268.1:p.Ile174Ser
NM_001354304.1:c.521T>G NP_001341233.1:p.Ile174Ser
XM_017019370.2:c.521T>G XP_016874859.1:p.Ile174Ser
NM_000277.3:c.521T>G MANE Select NP_000268.1:p.Ile174Ser
NM_001354304.2:c.521T>G NP_001341233.1:p.Ile174Ser
Search 100 bp 5'
Search 100 bp 3'