Canonical Allele Identifier: CA2610266835
Gene: CYP2C9 HGNC NCBI

Linked Data

gnomAD v4: 10-94988983-T-TGCC
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988984_94988986dup , CM000672.2:g.94988984_94988986dup GRCh38
NC_000010.10:g.96748741_96748743dup , CM000672.1:g.96748741_96748743dup GRCh37
NC_000010.9:g.96738731_96738733dup NCBI36
NG_008385.1:g.55327_55329dup
NG_008385.2:g.55827_55829dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1429_1431dup MANE Select ENSP00000260682.6:p.Ala477_Ser478insAla
ENST00000643112.1:c.*438_*440dup ENSP00000496202.1:n.*438_*440dup
ENST00000260682.6:c.1429_1431dup ENSP00000260682.6:p.Ala477_Ser478insAla
NM_000771.3:c.1429_1431dup NP_000762.2:p.Ala477_Ser478insAla
NM_000771.4:c.1429_1431dup MANE Select NP_000762.2:p.Ala477_Ser478insAla
Search 100 bp 5'
Search 100 bp 3'