Canonical Allele Identifier: CA595314956
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1202816434
gnomAD v2: 10-96702482-G-A
gnomAD v3: 10-94942725-G-A
gnomAD v4: 10-94942725-G-A
MyVariant Identifiers: chr10:g.96702482G>A (hg19) chr10:g.94942725G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942725G>A , CM000672.2:g.94942725G>A GRCh38
NC_000010.10:g.96702482G>A , CM000672.1:g.96702482G>A GRCh37
NC_000010.9:g.96692472G>A NCBI36
NG_008385.1:g.9068G>A
NG_008385.2:g.9568G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.481+384G>A MANE Select ENSP00000260682.6:n.481+384G>A
ENST00000643112.1:c.481+384G>A ENSP00000496202.1:n.481+384G>A
ENST00000645207.1:n.634+384G>A
ENST00000260682.6:c.481+384G>A ENSP00000260682.6:n.481+384G>A
ENST00000461906.1:n.890G>A
ENST00000473496.1:n.252+384G>A
NM_000771.3:c.481+384G>A NP_000762.2:n.481+384G>A
NM_000771.4:c.481+384G>A MANE Select NP_000762.2:n.481+384G>A
Search 100 bp 5'
Search 100 bp 3'