Canonical Allele Identifier: CA2842321428
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989093T>G , CM000672.2:g.94989093T>G GRCh38
NC_000010.10:g.96748850T>G , CM000672.1:g.96748850T>G GRCh37
NC_000010.9:g.96738840T>G NCBI36
NG_008385.1:g.55436T>G
NG_008385.2:g.55936T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.*65T>G MANE Select ENSP00000260682.6:n.*65T>G
ENST00000643112.1:c.*547T>G ENSP00000496202.1:n.*547T>G
ENST00000260682.6:c.*65T>G ENSP00000260682.6:n.*65T>G
NM_000771.3:c.*65T>G NP_000762.2:n.*65T>G
NM_000771.4:c.*65T>G MANE Select NP_000762.2:n.*65T>G