Canonical Allele Identifier: CA5616399
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs769068984

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775383C>T , CM000672.2:g.94775383C>T GRCh38
NC_000010.10:g.96535140C>T , CM000672.1:g.96535140C>T GRCh37
NC_000010.9:g.96525130C>T NCBI36
NG_008384.2:g.17678C>T
NG_008384.3:g.17703C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.332-7C>T MANE Select ENSP00000360372.3:n.332-7C>T
ENST00000645461.1:n.1385-7C>T
ENST00000371321.7:c.332-7C>T ENSP00000360372.3:n.332-7C>T
ENST00000464755.1:c.1095-7C>T ENSP00000483243.1:n.1095-7C>T
ENST00000480405.2:c.332-7C>T ENSP00000483847.1:n.332-7C>T
NM_000769.2:c.332-7C>T NP_000760.1:n.332-7C>T
NM_000769.4:c.332-7C>T MANE Select NP_000760.1:n.332-7C>T