Canonical Allele Identifier: CA211696514
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1027843784

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852556C>T , CM000672.2:g.94852556C>T GRCh38
NC_000010.10:g.96612313C>T , CM000672.1:g.96612313C>T GRCh37
NC_000010.9:g.96602303C>T NCBI36
NG_008384.2:g.94851C>T
NG_008384.3:g.94876C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1292-177C>T MANE Select ENSP00000360372.3:n.1292-177C>T
ENST00000645461.1:n.2203-177C>T
ENST00000371321.7:c.1292-177C>T ENSP00000360372.3:n.1292-177C>T
ENST00000464755.1:c.2055-177C>T ENSP00000483243.1:n.2055-177C>T
NM_000769.2:c.1292-177C>T NP_000760.1:n.1292-177C>T
NM_000769.4:c.1292-177C>T MANE Select NP_000760.1:n.1292-177C>T