Canonical Allele Identifier: CA481375351
Gene: PAH HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.103234224G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102840446G>C , CM000674.2:g.102840446G>C GRCh38
NC_000012.11:g.103234224G>C , CM000674.1:g.103234224G>C GRCh37
NC_000012.10:g.101758354G>C NCBI36
NG_008690.1:g.82157C>G
NG_008690.2:g.122965C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.1269C>G MANE Select ENSP00000448059.1:p.Val423=
ENST00000307000.7:c.1254C>G ENSP00000303500.2:p.Val418=
ENST00000551114.2:n.931C>G
ENST00000553106.5:c.1269C>G ENSP00000448059.1:p.Val423=
ENST00000635477.1:c.373C>G
ENST00000635528.1:n.784C>G
NM_000277.1:c.1269C>G NP_000268.1:p.Val423=
XM_011538422.1:c.1212C>G XP_011536724.1:p.Val404=
NM_000277.2:c.1269C>G NP_000268.1:p.Val423=
NM_001354304.1:c.1269C>G NP_001341233.1:p.Val423=
NM_000277.3:c.1269C>G MANE Select NP_000268.1:p.Val423=
NM_001354304.2:c.1269C>G NP_001341233.1:p.Val423=
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