Canonical Allele Identifier: CA2610267725

Gene: CYP2C9

Linked Data

• gnomAD v4: 10-94941791-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94941794del , CM000672.2:g.94941794del	GRCh38
NC_000010.10:g.96701551del , CM000672.1:g.96701551del	GRCh37
NC_000010.9:g.96691541del	NCBI36
NG_008385.1:g.8137del
NG_008385.2:g.8637del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.169-64del MANE Select	ENSP00000260682.6:n.169-64del
ENST00000643112.1:c.169-64del	ENSP00000496202.1:n.169-64del
ENST00000645207.1:n.258del
ENST00000260682.6:c.169-64del	ENSP00000260682.6:n.169-64del
ENST00000461906.1:n.194-64del
NM_000771.3:c.169-64del	NP_000762.2:n.169-64del
NM_000771.4:c.169-64del MANE Select	NP_000762.2:n.169-64del