Canonical Allele Identifier: CA377671226
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs2134240488

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781870A>C , CM000672.2:g.94781870A>C GRCh38
NC_000010.10:g.96541627A>C , CM000672.1:g.96541627A>C GRCh37
NC_000010.9:g.96531617A>C NCBI36
NG_008384.2:g.24165A>C
NG_008384.3:g.24190A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.692A>C MANE Select ENSP00000360372.3:p.Asn231Thr
ENST00000645461.1:n.1745A>C
ENST00000371321.7:c.692A>C ENSP00000360372.3:p.Asn231Thr
ENST00000464755.1:c.1455A>C ENSP00000483243.1:n.1455A>C
NM_000769.2:c.692A>C NP_000760.1:p.Asn231Thr
NM_000769.4:c.692A>C MANE Select NP_000760.1:p.Asn231Thr