Canonical Allele Identifier: CA242484904
Gene: PAH HGNC NCBI

Linked Data

dbSNP Id: rs1025156786
gnomAD v3: 12-102866024-A-T
gnomAD v4: 12-102866024-A-T
MyVariant Identifiers: chr12:g.103259802A>T (hg19) chr12:g.102866024A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102866024A>T , CM000674.2:g.102866024A>T GRCh38
NC_000012.11:g.103259802A>T , CM000674.1:g.103259802A>T GRCh37
NC_000012.10:g.101783932A>T NCBI36
NG_008690.1:g.56579T>A
NG_008690.2:g.97387T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.509+572T>A MANE Select ENSP00000448059.1:n.509+572T>A
ENST00000307000.7:c.494+572T>A ENSP00000303500.2:n.494+572T>A
ENST00000549111.5:n.605+572T>A
ENST00000551988.5:n.531-10692T>A
ENST00000553106.5:c.509+572T>A ENSP00000448059.1:n.509+572T>A
NM_000277.1:c.509+572T>A NP_000268.1:n.509+572T>A
XM_011538422.1:c.509+572T>A XP_011536724.1:n.509+572T>A
NM_000277.2:c.509+572T>A NP_000268.1:n.509+572T>A
NM_001354304.1:c.509+572T>A NP_001341233.1:n.509+572T>A
XM_017019370.2:c.509+572T>A XP_016874859.1:n.509+572T>A
NM_000277.3:c.509+572T>A MANE Select NP_000268.1:n.509+572T>A
NM_001354304.2:c.509+572T>A NP_001341233.1:n.509+572T>A
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