Canonical Allele Identifier: CA670159341

Gene: CYP2C9

Linked Data

• dbSNP Id: rs1337281779
• gnomAD v4: 10-94942749-G-T
• MyVariant Identifiers: chr10:g.96702506G>T (hg19) ; chr10:g.94942749G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94942749G>T , CM000672.2:g.94942749G>T	GRCh38
NC_000010.10:g.96702506G>T , CM000672.1:g.96702506G>T	GRCh37
NC_000010.9:g.96692496G>T	NCBI36
NG_008385.1:g.9092G>T
NG_008385.2:g.9592G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.481+408G>T MANE Select	ENSP00000260682.6:n.481+408G>T
ENST00000643112.1:c.481+408G>T	ENSP00000496202.1:n.481+408G>T
ENST00000645207.1:n.634+408G>T
ENST00000260682.6:c.481+408G>T	ENSP00000260682.6:n.481+408G>T
ENST00000461906.1:n.914G>T
ENST00000473496.1:n.252+408G>T
NM_000771.3:c.481+408G>T	NP_000762.2:n.481+408G>T
NM_000771.4:c.481+408G>T MANE Select	NP_000762.2:n.481+408G>T