Canonical Allele Identifier: CA5616268

Gene: CYP2C19

Linked Data

• dbSNP Id: rs771935348
• ExAC: 10:96522419 G / T
• gnomAD v4: 10-94762662-G-T
• MyVariant Identifiers: chr10:g.96522419G>T (hg19) ; chr10:g.94762662G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94762662G>T , CM000672.2:g.94762662G>T	GRCh38
NC_000010.10:g.96522419G>T , CM000672.1:g.96522419G>T	GRCh37
NC_000010.9:g.96512409G>T	NCBI36
NG_008384.2:g.4957G>T
NG_008384.3:g.4982G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371321.7:c.-44G>T	ENSP00000360372.3:n.-44G>T
ENST00000464755.1:c.932-12396G>T	ENSP00000483243.1:n.932-12396G>T