Canonical Allele Identifier: CA595638644

Gene: CYP2C19

Linked Data

• dbSNP Id: rs1163276252
• gnomAD v2: 10-96535025-G-C
• gnomAD v3: 10-94775268-G-C
• gnomAD v4: 10-94775268-G-C
• MyVariant Identifiers: chr10:g.96535025G>C (hg19) ; chr10:g.94775268G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94775268G>C , CM000672.2:g.94775268G>C	GRCh38
NC_000010.10:g.96535025G>C , CM000672.1:g.96535025G>C	GRCh37
NC_000010.9:g.96525015G>C	NCBI36
NG_008384.2:g.17563G>C
NG_008384.3:g.17588G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371321.9:c.331+48G>C MANE Select	ENSP00000360372.3:n.331+48G>C
ENST00000645461.1:n.1384+48G>C
ENST00000371321.7:c.331+48G>C	ENSP00000360372.3:n.331+48G>C
ENST00000464755.1:c.1094+48G>C	ENSP00000483243.1:n.1094+48G>C
ENST00000480405.2:c.331+48G>C	ENSP00000483847.1:n.331+48G>C
NM_000769.2:c.331+48G>C	NP_000760.1:n.331+48G>C
NM_000769.4:c.331+48G>C MANE Select	NP_000760.1:n.331+48G>C