Canonical Allele Identifier: CA5617432

Gene: CYP2C9

Linked Data

• dbSNP Id: rs375918804
• ExAC: 10:96748818 G / A
• gnomAD v2: 10-96748818-G-A
• gnomAD v3: 10-94989061-G-A
• gnomAD v4: 10-94989061-G-A
• MyVariant Identifiers: chr10:g.96748818G>A (hg19) ; chr10:g.94989061G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94989061G>A , CM000672.2:g.94989061G>A	GRCh38
NC_000010.10:g.96748818G>A , CM000672.1:g.96748818G>A	GRCh37
NC_000010.9:g.96738808G>A	NCBI36
NG_008385.1:g.55404G>A
NG_008385.2:g.55904G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000260682.8:c.*33G>A MANE Select	ENSP00000260682.6:n.*33G>A
ENST00000643112.1:c.*515G>A	ENSP00000496202.1:n.*515G>A
ENST00000260682.6:c.*33G>A	ENSP00000260682.6:n.*33G>A
NM_000771.3:c.*33G>A	NP_000762.2:n.*33G>A
NM_000771.4:c.*33G>A MANE Select	NP_000762.2:n.*33G>A