Canonical Allele Identifier: CA2610267798
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942324_94942389del , CM000672.2:g.94942324_94942389del GRCh38
NC_000010.10:g.96702081_96702146del , CM000672.1:g.96702081_96702146del GRCh37
NC_000010.9:g.96692071_96692136del NCBI36
NG_008385.1:g.8667_8732del
NG_008385.2:g.9167_9232del

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.464_481+48del
ENST00000643112.1:c.464_481+48del
ENST00000645207.1:n.617_634+48del
ENST00000260682.6:c.464_481+48del
ENST00000461906.1:n.489_554del
ENST00000473496.1:n.235_252+48del
NM_000771.3:c.464_481+48del
NM_000771.4:c.464_481+48del