Canonical Allele Identifier: CA1929342522
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs967063988
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981617C>A , CM000672.2:g.94981617C>A GRCh38
NC_000010.10:g.96741374C>A , CM000672.1:g.96741374C>A GRCh37
NC_000010.9:g.96731364C>A NCBI36
NG_008385.1:g.47960C>A
NG_008385.2:g.48460C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1149+247C>A MANE Select ENSP00000260682.6:n.1149+247C>A
ENST00000643112.1:c.*158+247C>A ENSP00000496202.1:n.*158+247C>A
ENST00000260682.6:c.1149+247C>A ENSP00000260682.6:n.1149+247C>A
NM_000771.3:c.1149+247C>A NP_000762.2:n.1149+247C>A
NM_000771.4:c.1149+247C>A MANE Select NP_000762.2:n.1149+247C>A
Search 100 bp 5'
Search 100 bp 3'