Canonical Allele Identifier: CA1929349382
Gene: CYP2C9 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988804T= , CM000672.2:g.94988804T= GRCh38
NC_000010.10:g.96748561T= , CM000672.1:g.96748561T= GRCh37
NC_000010.9:g.96738551T= NCBI36
NG_008385.1:g.55147T=
NG_008385.2:g.55647T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1292-43T= MANE Select ENSP00000260682.6:n.1292-43T=
ENST00000643112.1:c.*301-43T= ENSP00000496202.1:n.*301-43T=
ENST00000260682.6:c.1292-43T= ENSP00000260682.6:n.1292-43T=
NM_000771.3:c.1292-43T= NP_000762.2:n.1292-43T=
NM_000771.4:c.1292-43T= MANE Select NP_000762.2:n.1292-43T=
Search 100 bp 5'
Search 100 bp 3'