Canonical Allele Identifier: CA1929292582
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs2031410398
gnomAD v4: 10-94942552-TA-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942556del , CM000672.2:g.94942556del GRCh38
NC_000010.10:g.96702313del , CM000672.1:g.96702313del GRCh37
NC_000010.9:g.96692303del NCBI36
NG_008385.1:g.8899del
NG_008385.2:g.9399del

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.481+215del MANE Select ENSP00000260682.6:n.481+215del
ENST00000643112.1:c.481+215del ENSP00000496202.1:n.481+215del
ENST00000645207.1:n.634+215del
ENST00000260682.6:c.481+215del ENSP00000260682.6:n.481+215del
ENST00000461906.1:n.721del
ENST00000473496.1:n.252+215del
NM_000771.3:c.481+215del NP_000762.2:n.481+215del
NM_000771.4:c.481+215del MANE Select NP_000762.2:n.481+215del
Search 100 bp 5'
Search 100 bp 3'