Canonical Allele Identifier: CA386296693
Gene: PAH HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.103248997T>G (hg19) chr12:g.102855219T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102855219T>G , CM000674.2:g.102855219T>G GRCh38
NC_000012.11:g.103248997T>G , CM000674.1:g.103248997T>G GRCh37
NC_000012.10:g.101773127T>G NCBI36
NG_008690.1:g.67384A>C
NG_008690.2:g.108192A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.623A>C MANE Select ENSP00000448059.1:p.His208Pro
ENST00000307000.7:c.608A>C ENSP00000303500.2:p.His203Pro
ENST00000549111.5:n.719A>C
ENST00000553106.5:c.623A>C ENSP00000448059.1:p.His208Pro
NM_000277.1:c.623A>C NP_000268.1:p.His208Pro
XM_011538422.1:c.623A>C XP_011536724.1:p.His208Pro
NM_000277.2:c.623A>C NP_000268.1:p.His208Pro
NM_001354304.1:c.623A>C NP_001341233.1:p.His208Pro
XM_017019370.2:c.623A>C XP_016874859.1:p.His208Pro
NM_000277.3:c.623A>C MANE Select NP_000268.1:p.His208Pro
NM_001354304.2:c.623A>C NP_001341233.1:p.His208Pro
Search 100 bp 5'
Search 100 bp 3'