Canonical Allele Identifier: CA377676234

Gene: CYP2C9

Linked Data

• gnomAD v4: 10-94981238-G-T
• MyVariant Identifiers: chr10:g.96740995G>T (hg19) ; chr10:g.94981238G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94981238G>T , CM000672.2:g.94981238G>T	GRCh38
NC_000010.10:g.96740995G>T , CM000672.1:g.96740995G>T	GRCh37
NC_000010.9:g.96730985G>T	NCBI36
NG_008385.1:g.47581G>T
NG_008385.2:g.48081G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.1017G>T MANE Select	ENSP00000260682.6:p.Met339Ile
ENST00000643112.1:c.*26G>T	ENSP00000496202.1:n.*26G>T
ENST00000260682.6:c.1017G>T	ENSP00000260682.6:p.Met339Ile
NM_000771.3:c.1017G>T	NP_000762.2:p.Met339Ile
NM_000771.4:c.1017G>T MANE Select	NP_000762.2:p.Met339Ile