Canonical Allele Identifier: CA377675097
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94849990A>C , CM000672.2:g.94849990A>C GRCh38
NC_000010.10:g.96609747A>C , CM000672.1:g.96609747A>C GRCh37
NC_000010.9:g.96599737A>C NCBI36
NG_008384.2:g.92285A>C
NG_008384.3:g.92310A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1223A>C MANE Select ENSP00000360372.3:p.Asp408Ala
ENST00000645461.1:n.2134A>C
ENST00000371321.7:c.1223A>C ENSP00000360372.3:p.Asp408Ala
ENST00000464755.1:c.1986A>C ENSP00000483243.1:n.1986A>C
NM_000769.2:c.1223A>C NP_000760.1:p.Asp408Ala
NM_000769.4:c.1223A>C MANE Select NP_000760.1:p.Asp408Ala