Canonical Allele Identifier: CA1929334823
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs2032097396

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94974528T>G , CM000672.2:g.94974528T>G GRCh38
NC_000010.10:g.96734285T>G , CM000672.1:g.96734285T>G GRCh37
NC_000010.9:g.96724275T>G NCBI36
NG_008385.1:g.40871T>G
NG_008385.2:g.41371T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.961+2283T>G MANE Select ENSP00000260682.6:n.961+2283T>G
ENST00000643112.1:c.820-6655T>G ENSP00000496202.1:n.820-6655T>G
ENST00000260682.6:c.961+2283T>G ENSP00000260682.6:n.961+2283T>G
NM_000771.3:c.961+2283T>G NP_000762.2:n.961+2283T>G
NM_000771.4:c.961+2283T>G MANE Select NP_000762.2:n.961+2283T>G