Canonical Allele Identifier: CA5617261
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs756602662

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981157A>G , CM000672.2:g.94981157A>G GRCh38
NC_000010.10:g.96740914A>G , CM000672.1:g.96740914A>G GRCh37
NC_000010.9:g.96730904A>G NCBI36
NG_008385.1:g.47500A>G
NG_008385.2:g.48000A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.962-26A>G MANE Select ENSP00000260682.6:n.962-26A>G
ENST00000643112.1:c.820-26A>G ENSP00000496202.1:n.820-26A>G
ENST00000260682.6:c.962-26A>G ENSP00000260682.6:n.962-26A>G
NM_000771.3:c.962-26A>G NP_000762.2:n.962-26A>G
NM_000771.4:c.962-26A>G MANE Select NP_000762.2:n.962-26A>G