Canonical Allele Identifier: CA5616429
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs763625282

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775465T>C , CM000672.2:g.94775465T>C GRCh38
NC_000010.10:g.96535222T>C , CM000672.1:g.96535222T>C GRCh37
NC_000010.9:g.96525212T>C NCBI36
NG_008384.2:g.17760T>C
NG_008384.3:g.17785T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.407T>C MANE Select ENSP00000360372.3:p.Met136Thr
ENST00000645461.1:n.1460T>C
ENST00000371321.7:c.407T>C ENSP00000360372.3:p.Met136Thr
ENST00000464755.1:c.1170T>C ENSP00000483243.1:n.1170T>C
ENST00000480405.2:c.407T>C ENSP00000483847.1:p.Met136Thr
NM_000769.2:c.407T>C NP_000760.1:p.Met136Thr
NM_000769.4:c.407T>C MANE Select NP_000760.1:p.Met136Thr