Canonical Allele Identifier: CA377675143
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1468400400

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94850013G>A , CM000672.2:g.94850013G>A GRCh38
NC_000010.10:g.96609770G>A , CM000672.1:g.96609770G>A GRCh37
NC_000010.9:g.96599760G>A NCBI36
NG_008384.2:g.92308G>A
NG_008384.3:g.92333G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1246G>A MANE Select ENSP00000360372.3:p.Gly416Ser
ENST00000645461.1:n.2157G>A
ENST00000371321.7:c.1246G>A ENSP00000360372.3:p.Gly416Ser
ENST00000464755.1:c.2009G>A ENSP00000483243.1:n.2009G>A
NM_000769.2:c.1246G>A NP_000760.1:p.Gly416Ser
NM_000769.4:c.1246G>A MANE Select NP_000760.1:p.Gly416Ser