Canonical Allele Identifier: CA595638887
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1564722635
MyVariant Identifiers: chr10:g.96748826del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989069del , CM000672.2:g.94989069del GRCh38
NC_000010.10:g.96748826del , CM000672.1:g.96748826del GRCh37
NC_000010.9:g.96738816del NCBI36
NG_008385.1:g.55412del
NG_008385.2:g.55912del

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.*41del MANE Select ENSP00000260682.6:n.*41del
ENST00000643112.1:c.*523del ENSP00000496202.1:n.*523del
ENST00000260682.6:c.*41del ENSP00000260682.6:n.*41del
NM_000771.3:c.*41del NP_000762.2:n.*41del
NM_000771.4:c.*41del MANE Select NP_000762.2:n.*41del