Canonical Allele Identifier: CA2789073509
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94974462G>T , CM000672.2:g.94974462G>T GRCh38
NC_000010.10:g.96734219G>T , CM000672.1:g.96734219G>T GRCh37
NC_000010.9:g.96724209G>T NCBI36
NG_008385.1:g.40805G>T
NG_008385.2:g.41305G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.961+2217G>T MANE Select ENSP00000260682.6:n.961+2217G>T
ENST00000643112.1:c.820-6721G>T ENSP00000496202.1:n.820-6721G>T
ENST00000260682.6:c.961+2217G>T ENSP00000260682.6:n.961+2217G>T
NM_000771.3:c.961+2217G>T NP_000762.2:n.961+2217G>T
NM_000771.4:c.961+2217G>T MANE Select NP_000762.2:n.961+2217G>T