Canonical Allele Identifier: CA931377485
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1848464201

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780410A>C , CM000672.2:g.94780410A>C GRCh38
NC_000010.10:g.96540167A>C , CM000672.1:g.96540167A>C GRCh37
NC_000010.9:g.96530157A>C NCBI36
NG_008384.2:g.22705A>C
NG_008384.3:g.22730A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.482-89A>C MANE Select ENSP00000360372.3:n.482-89A>C
ENST00000645461.1:n.1535-89A>C
ENST00000371321.7:c.482-89A>C ENSP00000360372.3:n.482-89A>C
ENST00000464755.1:c.1245-89A>C ENSP00000483243.1:n.1245-89A>C
NM_000769.2:c.482-89A>C NP_000760.1:n.482-89A>C
NM_000769.4:c.482-89A>C MANE Select NP_000760.1:n.482-89A>C