Canonical Allele Identifier: CA377670491
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1406158087

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780537C>T , CM000672.2:g.94780537C>T GRCh38
NC_000010.10:g.96540294C>T , CM000672.1:g.96540294C>T GRCh37
NC_000010.9:g.96530284C>T NCBI36
NG_008384.2:g.22832C>T
NG_008384.3:g.22857C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.520C>T MANE Select ENSP00000360372.3:p.Pro174Ser
ENST00000645461.1:n.1573C>T
ENST00000371321.7:c.520C>T ENSP00000360372.3:p.Pro174Ser
ENST00000464755.1:c.1283C>T ENSP00000483243.1:n.1283C>T
NM_000769.2:c.520C>T NP_000760.1:p.Pro174Ser
NM_000769.4:c.520C>T MANE Select NP_000760.1:p.Pro174Ser