Canonical Allele Identifier: CA5616516

Gene: CYP2C19

Linked Data

• dbSNP Id: rs57752480
• ExAC: 10:96541538 T / C
• gnomAD v2: 10-96541538-T-C
• gnomAD v3: 10-94781781-T-C
• gnomAD v4: 10-94781781-T-C
• MyVariant Identifiers: chr10:g.96541538T>C (hg19) ; chr10:g.94781781T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94781781T>C , CM000672.2:g.94781781T>C	GRCh38
NC_000010.10:g.96541538T>C , CM000672.1:g.96541538T>C	GRCh37
NC_000010.9:g.96531528T>C	NCBI36
NG_008384.2:g.24076T>C
NG_008384.3:g.24101T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.643-40T>C MANE Select	ENSP00000360372.3:n.643-40T>C
ENST00000645461.1:n.1696-40T>C
ENST00000371321.7:c.643-40T>C	ENSP00000360372.3:n.643-40T>C
ENST00000464755.1:c.1406-40T>C	ENSP00000483243.1:n.1406-40T>C
NM_000769.2:c.643-40T>C	NP_000760.1:n.643-40T>C
NM_000769.4:c.643-40T>C MANE Select	NP_000760.1:n.643-40T>C