Canonical Allele Identifier: CA5616389

Gene: CYP2C19

Linked Data

• dbSNP Id: rs374825809
• ExAC: 10:96535112 G / T
• gnomAD v2: 10-96535112-G-T
• gnomAD v3: 10-94775355-G-T
• gnomAD v4: 10-94775355-G-T
• MyVariant Identifiers: chr10:g.96535112G>T (hg19) ; chr10:g.94775355G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94775355G>T , CM000672.2:g.94775355G>T	GRCh38
NC_000010.10:g.96535112G>T , CM000672.1:g.96535112G>T	GRCh37
NC_000010.9:g.96525102G>T	NCBI36
NG_008384.2:g.17650G>T
NG_008384.3:g.17675G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371321.9:c.332-35G>T MANE Select	ENSP00000360372.3:n.332-35G>T
ENST00000645461.1:n.1385-35G>T
ENST00000371321.7:c.332-35G>T	ENSP00000360372.3:n.332-35G>T
ENST00000464755.1:c.1095-35G>T	ENSP00000483243.1:n.1095-35G>T
ENST00000480405.2:c.332-35G>T	ENSP00000483847.1:n.332-35G>T
NM_000769.2:c.332-35G>T	NP_000760.1:n.332-35G>T
NM_000769.4:c.332-35G>T MANE Select	NP_000760.1:n.332-35G>T