Canonical Allele Identifier: CA5617426
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs745770093
ExAC: 10:96748790 G / A
gnomAD v2: 10-96748790-G-A
gnomAD v4: 10-94989033-G-A
MyVariant Identifiers: chr10:g.96748790G>A (hg19) chr10:g.94989033G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989033G>A , CM000672.2:g.94989033G>A GRCh38
NC_000010.10:g.96748790G>A , CM000672.1:g.96748790G>A GRCh37
NC_000010.9:g.96738780G>A NCBI36
NG_008385.1:g.55376G>A
NG_008385.2:g.55876G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.*5G>A MANE Select ENSP00000260682.6:n.*5G>A
ENST00000643112.1:c.*487G>A ENSP00000496202.1:n.*487G>A
ENST00000260682.6:c.*5G>A ENSP00000260682.6:n.*5G>A
NM_000771.3:c.*5G>A NP_000762.2:n.*5G>A
NM_000771.4:c.*5G>A MANE Select NP_000762.2:n.*5G>A
Search 100 bp 5'
Search 100 bp 3'