Canonical Allele Identifier: CA5617259
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs765854686
ExAC: 10:96740906 C / A
gnomAD v2: 10-96740906-C-A
gnomAD v4: 10-94981149-C-A
MyVariant Identifiers: chr10:g.96740906C>A (hg19) chr10:g.94981149C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981149C>A , CM000672.2:g.94981149C>A GRCh38
NC_000010.10:g.96740906C>A , CM000672.1:g.96740906C>A GRCh37
NC_000010.9:g.96730896C>A NCBI36
NG_008385.1:g.47492C>A
NG_008385.2:g.47992C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.962-34C>A MANE Select ENSP00000260682.6:n.962-34C>A
ENST00000643112.1:c.820-34C>A ENSP00000496202.1:n.820-34C>A
ENST00000260682.6:c.962-34C>A ENSP00000260682.6:n.962-34C>A
NM_000771.3:c.962-34C>A NP_000762.2:n.962-34C>A
NM_000771.4:c.962-34C>A MANE Select NP_000762.2:n.962-34C>A
Search 100 bp 5'
Search 100 bp 3'