Canonical Allele Identifier: CA377667822
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762733T>A , CM000672.2:g.94762733T>A GRCh38
NC_000010.10:g.96522490T>A , CM000672.1:g.96522490T>A GRCh37
NC_000010.9:g.96512480T>A NCBI36
NG_008384.2:g.5028T>A
NG_008384.3:g.5053T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.28T>A MANE Select ENSP00000360372.3:p.Cys10Ser
ENST00000371321.7:c.28T>A ENSP00000360372.3:p.Cys10Ser
ENST00000464755.1:c.932-12325T>A ENSP00000483243.1:n.932-12325T>A
ENST00000480405.2:c.28T>A ENSP00000483847.1:p.Cys10Ser
NM_000769.2:c.28T>A NP_000760.1:p.Cys10Ser
NM_000769.4:c.28T>A MANE Select NP_000760.1:p.Cys10Ser