Canonical Allele Identifier: CA211724801
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1047915522
gnomAD v3: 10-94974655-G-A
gnomAD v4: 10-94974655-G-A
MyVariant Identifiers: chr10:g.96734412G>A (hg19) chr10:g.94974655G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94974655G>A , CM000672.2:g.94974655G>A GRCh38
NC_000010.10:g.96734412G>A , CM000672.1:g.96734412G>A GRCh37
NC_000010.9:g.96724402G>A NCBI36
NG_008385.1:g.40998G>A
NG_008385.2:g.41498G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.961+2410G>A MANE Select ENSP00000260682.6:n.961+2410G>A
ENST00000643112.1:c.820-6528G>A ENSP00000496202.1:n.820-6528G>A
ENST00000260682.6:c.961+2410G>A ENSP00000260682.6:n.961+2410G>A
NM_000771.3:c.961+2410G>A NP_000762.2:n.961+2410G>A
NM_000771.4:c.961+2410G>A MANE Select NP_000762.2:n.961+2410G>A
Search 100 bp 5'
Search 100 bp 3'