Canonical Allele Identifier: CA377672732

Gene: CYP2C9

Linked Data

• MyVariant Identifiers: chr10:g.96701669G>T (hg19) ; chr10:g.94941912G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94941912G>T , CM000672.2:g.94941912G>T	GRCh38
NC_000010.10:g.96701669G>T , CM000672.1:g.96701669G>T	GRCh37
NC_000010.9:g.96691659G>T	NCBI36
NG_008385.1:g.8255G>T
NG_008385.2:g.8755G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.223G>T MANE Select	ENSP00000260682.6:p.Val75Leu
ENST00000643112.1:c.223G>T	ENSP00000496202.1:p.Val75Leu
ENST00000645207.1:n.376G>T
ENST00000260682.6:c.223G>T	ENSP00000260682.6:p.Val75Leu
ENST00000461906.1:n.248G>T
NM_000771.3:c.223G>T	NP_000762.2:p.Val75Leu
NM_000771.4:c.223G>T MANE Select	NP_000762.2:p.Val75Leu