Canonical Allele Identifier: CA1929341839
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981154T= , CM000672.2:g.94981154T= GRCh38
NC_000010.10:g.96740911T= , CM000672.1:g.96740911T= GRCh37
NC_000010.9:g.96730901T= NCBI36
NG_008385.1:g.47497T=
NG_008385.2:g.47997T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.962-29T= MANE Select ENSP00000260682.6:n.962-29T=
ENST00000643112.1:c.820-29T= ENSP00000496202.1:n.820-29T=
ENST00000260682.6:c.962-29T= ENSP00000260682.6:n.962-29T=
NM_000771.3:c.962-29T= NP_000762.2:n.962-29T=
NM_000771.4:c.962-29T= MANE Select NP_000762.2:n.962-29T=