Canonical Allele Identifier: CA377669643
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1848389182

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775140A>C , CM000672.2:g.94775140A>C GRCh38
NC_000010.10:g.96534897A>C , CM000672.1:g.96534897A>C GRCh37
NC_000010.9:g.96524887A>C NCBI36
NG_008384.2:g.17435A>C
NG_008384.3:g.17460A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.251A>C MANE Select ENSP00000360372.3:p.Lys84Thr
ENST00000645461.1:n.1304A>C
ENST00000371321.7:c.251A>C ENSP00000360372.3:p.Lys84Thr
ENST00000464755.1:c.1014A>C ENSP00000483243.1:n.1014A>C
ENST00000480405.2:c.251A>C ENSP00000483847.1:p.Lys84Thr
NM_000769.2:c.251A>C NP_000760.1:p.Lys84Thr
NM_000769.4:c.251A>C MANE Select NP_000760.1:p.Lys84Thr