Canonical Allele Identifier: CA2610267722
Gene: CYP2C9 HGNC NCBI

Linked Data

gnomAD v4: 10-94941787-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94941787A>G , CM000672.2:g.94941787A>G GRCh38
NC_000010.10:g.96701544A>G , CM000672.1:g.96701544A>G GRCh37
NC_000010.9:g.96691534A>G NCBI36
NG_008385.1:g.8130A>G
NG_008385.2:g.8630A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.169-71A>G MANE Select ENSP00000260682.6:n.169-71A>G
ENST00000643112.1:c.169-71A>G ENSP00000496202.1:n.169-71A>G
ENST00000645207.1:n.251A>G
ENST00000260682.6:c.169-71A>G ENSP00000260682.6:n.169-71A>G
ENST00000461906.1:n.194-71A>G
NM_000771.3:c.169-71A>G NP_000762.2:n.169-71A>G
NM_000771.4:c.169-71A>G MANE Select NP_000762.2:n.169-71A>G
Search 100 bp 5'
Search 100 bp 3'