Canonical Allele Identifier: CA2610266786
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988743del , CM000672.2:g.94988743del GRCh38
NC_000010.10:g.96748500del , CM000672.1:g.96748500del GRCh37
NC_000010.9:g.96738490del NCBI36
NG_008385.1:g.55086del
NG_008385.2:g.55586del

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1292-104del MANE Select ENSP00000260682.6:n.1292-104del
ENST00000643112.1:c.*301-104del ENSP00000496202.1:n.*301-104del
ENST00000260682.6:c.1292-104del ENSP00000260682.6:n.1292-104del
NM_000771.3:c.1292-104del NP_000762.2:n.1292-104del
NM_000771.4:c.1292-104del MANE Select NP_000762.2:n.1292-104del