Canonical Allele Identifier: CA386296633
Gene: PAH HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.103248969A>T (hg19) chr12:g.102855191A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102855191A>T , CM000674.2:g.102855191A>T GRCh38
NC_000012.11:g.103248969A>T , CM000674.1:g.103248969A>T GRCh37
NC_000012.10:g.101773099A>T NCBI36
NG_008690.1:g.67412T>A
NG_008690.2:g.108220T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.651T>A MANE Select ENSP00000448059.1:p.Cys217Ter
ENST00000307000.7:c.636T>A ENSP00000303500.2:p.Cys212Ter
ENST00000549111.5:n.747T>A
ENST00000553106.5:c.651T>A ENSP00000448059.1:p.Cys217Ter
NM_000277.1:c.651T>A NP_000268.1:p.Cys217Ter
XM_011538422.1:c.651T>A XP_011536724.1:p.Cys217Ter
NM_000277.2:c.651T>A NP_000268.1:p.Cys217Ter
NM_001354304.1:c.651T>A NP_001341233.1:p.Cys217Ter
XM_017019370.2:c.651T>A XP_016874859.1:p.Cys217Ter
NM_000277.3:c.651T>A MANE Select NP_000268.1:p.Cys217Ter
NM_001354304.2:c.651T>A NP_001341233.1:p.Cys217Ter
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