Canonical Allele Identifier: CA470987367
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1848393922
MyVariant Identifiers: chr10:g.96535169G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775412G>A , CM000672.2:g.94775412G>A GRCh38
NC_000010.10:g.96535169G>A , CM000672.1:g.96535169G>A GRCh37
NC_000010.9:g.96525159G>A NCBI36
NG_008384.2:g.17707G>A
NG_008384.3:g.17732G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.354G>A MANE Select ENSP00000360372.3:p.Lys118=
ENST00000645461.1:n.1407G>A
ENST00000371321.7:c.354G>A ENSP00000360372.3:p.Lys118=
ENST00000464755.1:c.1117G>A ENSP00000483243.1:n.1117G>A
ENST00000480405.2:c.354G>A ENSP00000483847.1:p.Lys118=
NM_000769.2:c.354G>A NP_000760.1:p.Lys118=
NM_000769.4:c.354G>A MANE Select NP_000760.1:p.Lys118=