Canonical Allele Identifier: CA5616375

Gene: CYP2C19

Linked Data

• dbSNP Id: rs199549982
• ExAC: 10:96534993 C / T
• gnomAD v2: 10-96534993-C-T
• gnomAD v3: 10-94775236-C-T
• gnomAD v4: 10-94775236-C-T
• MyVariant Identifiers: chr10:g.96534993C>T (hg19) ; chr10:g.94775236C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94775236C>T , CM000672.2:g.94775236C>T	GRCh38
NC_000010.10:g.96534993C>T , CM000672.1:g.96534993C>T	GRCh37
NC_000010.9:g.96524983C>T	NCBI36
NG_008384.2:g.17531C>T
NG_008384.3:g.17556C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371321.9:c.331+16C>T MANE Select	ENSP00000360372.3:n.331+16C>T
ENST00000645461.1:n.1384+16C>T
ENST00000371321.7:c.331+16C>T	ENSP00000360372.3:n.331+16C>T
ENST00000464755.1:c.1094+16C>T	ENSP00000483243.1:n.1094+16C>T
ENST00000480405.2:c.331+16C>T	ENSP00000483847.1:n.331+16C>T
NM_000769.2:c.331+16C>T	NP_000760.1:n.331+16C>T
NM_000769.4:c.331+16C>T MANE Select	NP_000760.1:n.331+16C>T