Canonical Allele Identifier: CA670182643
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1053204288

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981128C>G , CM000672.2:g.94981128C>G GRCh38
NC_000010.10:g.96740885C>G , CM000672.1:g.96740885C>G GRCh37
NC_000010.9:g.96730875C>G NCBI36
NG_008385.1:g.47471C>G
NG_008385.2:g.47971C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.962-55C>G MANE Select ENSP00000260682.6:n.962-55C>G
ENST00000643112.1:c.820-55C>G ENSP00000496202.1:n.820-55C>G
ENST00000260682.6:c.962-55C>G ENSP00000260682.6:n.962-55C>G
NM_000771.3:c.962-55C>G NP_000762.2:n.962-55C>G
NM_000771.4:c.962-55C>G MANE Select NP_000762.2:n.962-55C>G