Canonical Allele Identifier: CA386294528
Gene: PAH HGNC NCBI

Linked Data

dbSNP Id: rs199475654
gnomAD v4: 12-102852816-G-T
MyVariant Identifiers: chr12:g.103246594G>T (hg19) chr12:g.102852816G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102852816G>T , CM000674.2:g.102852816G>T GRCh38
NC_000012.11:g.103246594G>T , CM000674.1:g.103246594G>T GRCh37
NC_000012.10:g.101770724G>T NCBI36
NG_008690.1:g.69787C>A
NG_008690.2:g.110595C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.841C>A MANE Select ENSP00000448059.1:p.Pro281Thr
ENST00000307000.7:c.826C>A ENSP00000303500.2:p.Pro276Thr
ENST00000549247.6:n.600C>A
ENST00000553106.5:c.841C>A ENSP00000448059.1:p.Pro281Thr
ENST00000635477.1:c.2C>A
NM_000277.1:c.841C>A NP_000268.1:p.Pro281Thr
XM_011538422.1:c.841C>A XP_011536724.1:p.Pro281Thr
NM_000277.2:c.841C>A NP_000268.1:p.Pro281Thr
NM_001354304.1:c.841C>A NP_001341233.1:p.Pro281Thr
NM_000277.3:c.841C>A MANE Select NP_000268.1:p.Pro281Thr
NM_001354304.2:c.841C>A NP_001341233.1:p.Pro281Thr
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