Canonical Allele Identifier: CA5616409
Gene: CYP2C19 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 39351
ClinVar RCV Id: RCV000394401
dbSNP Id: rs41291556

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775416T>C , CM000672.2:g.94775416T>C GRCh38
NC_000010.10:g.96535173T>C , CM000672.1:g.96535173T>C GRCh37
NC_000010.9:g.96525163T>C NCBI36
NG_008384.2:g.17711T>C
NG_008384.3:g.17736T>C

Transcript Alleles

HGVS Amino-acid change
NM_000769.2:c.358T>C VV NP_000760.1:p.Trp120Arg
NM_000769.4:c.358T>C VV MANE Preferred NP_000760.1:p.Trp120Arg
ENST00000371321.7:c.358T>C ENSP00000360372.3:p.Trp120Arg
ENST00000464755.1:n.1121T>C ENSP00000483243.1:p.=
ENST00000480405.2:c.358T>C ENSP00000483847.1:p.Trp120Arg