Canonical Allele Identifier: CA377672922

Gene: CYP2C9

Linked Data

• gnomAD v4: 10-94942005-G-C
• MyVariant Identifiers: chr10:g.96701762G>C (hg19) ; chr10:g.94942005G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94942005G>C , CM000672.2:g.94942005G>C	GRCh38
NC_000010.10:g.96701762G>C , CM000672.1:g.96701762G>C	GRCh37
NC_000010.9:g.96691752G>C	NCBI36
NG_008385.1:g.8348G>C
NG_008385.2:g.8848G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.316G>C MANE Select	ENSP00000260682.6:p.Ala106Pro
ENST00000643112.1:c.316G>C	ENSP00000496202.1:p.Ala106Pro
ENST00000645207.1:n.469G>C
ENST00000260682.6:c.316G>C	ENSP00000260682.6:p.Ala106Pro
ENST00000461906.1:n.341G>C
ENST00000473496.1:n.87G>C
NM_000771.3:c.316G>C	NP_000762.2:p.Ala106Pro
NM_000771.4:c.316G>C MANE Select	NP_000762.2:p.Ala106Pro