Canonical Allele Identifier: CA670164154
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1392804144

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780456T>C , CM000672.2:g.94780456T>C GRCh38
NC_000010.10:g.96540213T>C , CM000672.1:g.96540213T>C GRCh37
NC_000010.9:g.96530203T>C NCBI36
NG_008384.2:g.22751T>C
NG_008384.3:g.22776T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.482-43T>C MANE Select ENSP00000360372.3:n.482-43T>C
ENST00000645461.1:n.1535-43T>C
ENST00000371321.7:c.482-43T>C ENSP00000360372.3:n.482-43T>C
ENST00000464755.1:c.1245-43T>C ENSP00000483243.1:n.1245-43T>C
NM_000769.2:c.482-43T>C NP_000760.1:n.482-43T>C
NM_000769.4:c.482-43T>C MANE Select NP_000760.1:n.482-43T>C