Canonical Allele Identifier: CA377670416
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780499C>T , CM000672.2:g.94780499C>T GRCh38
NC_000010.10:g.96540256C>T , CM000672.1:g.96540256C>T GRCh37
NC_000010.9:g.96530246C>T NCBI36
NG_008384.2:g.22794C>T
NG_008384.3:g.22819C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.482C>T MANE Select ENSP00000360372.3:p.Ala161Val
ENST00000371321.7:c.482C>T ENSP00000360372.3:p.Ala161Val
ENST00000464755.1:n.1245C>T ENSP00000483243.1:p.=
NM_000769.2:c.482C>T NP_000760.1:p.Ala161Val
NM_000769.4:c.482C>T MANE Select NP_000760.1:p.Ala161Val