Canonical Allele Identifier: CA2610267683

Gene: CYP2C9

Linked Data

• gnomAD v4: 10-94941701-AATC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94941710_94941712del , CM000672.2:g.94941710_94941712del	GRCh38
NC_000010.10:g.96701467_96701469del , CM000672.1:g.96701467_96701469del	GRCh37
NC_000010.9:g.96691457_96691459del	NCBI36
NG_008385.1:g.8053_8055del
NG_008385.2:g.8553_8555del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.169-148_169-146del MANE Select	ENSP00000260682.6:n.169-148_169-146del
ENST00000643112.1:c.169-148_169-146del	ENSP00000496202.1:n.169-148_169-146del
ENST00000645207.1:n.174_176del
ENST00000260682.6:c.169-148_169-146del	ENSP00000260682.6:n.169-148_169-146del
ENST00000461906.1:n.194-148_194-146del
NM_000771.3:c.169-148_169-146del	NP_000762.2:n.169-148_169-146del
NM_000771.4:c.169-148_169-146del MANE Select	NP_000762.2:n.169-148_169-146del