Canonical Allele Identifier: CA377669861

Gene: CYP2C19

Linked Data

• gnomAD v4: 10-94775408-G-T
• MyVariant Identifiers: chr10:g.96535165G>T (hg19) ; chr10:g.94775408G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94775408G>T , CM000672.2:g.94775408G>T	GRCh38
NC_000010.10:g.96535165G>T , CM000672.1:g.96535165G>T	GRCh37
NC_000010.9:g.96525155G>T	NCBI36
NG_008384.2:g.17703G>T
NG_008384.3:g.17728G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371321.9:c.350G>T MANE Select	ENSP00000360372.3:p.Gly117Val
ENST00000645461.1:n.1403G>T
ENST00000371321.7:c.350G>T	ENSP00000360372.3:p.Gly117Val
ENST00000464755.1:c.1113G>T	ENSP00000483243.1:n.1113G>T
ENST00000480405.2:c.350G>T	ENSP00000483847.1:p.Gly117Val
NM_000769.2:c.350G>T	NP_000760.1:p.Gly117Val
NM_000769.4:c.350G>T MANE Select	NP_000760.1:p.Gly117Val