Canonical Allele Identifier: CA682823693
Gene: PAH HGNC NCBI

Linked Data

dbSNP Id: rs1291050218
gnomAD v3: 12-102844684-A-G
gnomAD v4: 12-102844684-A-G
MyVariant Identifiers: chr12:g.103238462A>G (hg19) chr12:g.102844684A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102844684A>G , CM000674.2:g.102844684A>G GRCh38
NC_000012.11:g.103238462A>G , CM000674.1:g.103238462A>G GRCh37
NC_000012.10:g.101762592A>G NCBI36
NG_008690.1:g.77919T>C
NG_008690.2:g.118727T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.970-253T>C MANE Select ENSP00000448059.1:n.970-253T>C
ENST00000307000.7:c.955-253T>C ENSP00000303500.2:n.955-253T>C
ENST00000549247.6:n.729-253T>C
ENST00000551114.2:n.632-253T>C
ENST00000553106.5:c.970-253T>C ENSP00000448059.1:n.970-253T>C
ENST00000635477.1:c.74-253T>C
ENST00000635528.1:n.485-253T>C
NM_000277.1:c.970-253T>C NP_000268.1:n.970-253T>C
XM_011538422.1:c.913-253T>C XP_011536724.1:n.913-253T>C
NM_000277.2:c.970-253T>C NP_000268.1:n.970-253T>C
NM_001354304.1:c.970-253T>C NP_001341233.1:n.970-253T>C
NM_000277.3:c.970-253T>C MANE Select NP_000268.1:n.970-253T>C
NM_001354304.2:c.970-253T>C NP_001341233.1:n.970-253T>C
Search 100 bp 5'
Search 100 bp 3'