Canonical Allele Identifier: CA377672639
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94941866G>T , CM000672.2:g.94941866G>T GRCh38
NC_000010.10:g.96701623G>T , CM000672.1:g.96701623G>T GRCh37
NC_000010.9:g.96691613G>T NCBI36
NG_008385.1:g.8209G>T
NG_008385.2:g.8709G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.177G>T MANE Select ENSP00000260682.6:p.Lys59Asn
ENST00000643112.1:c.177G>T ENSP00000496202.1:p.Lys59Asn
ENST00000645207.1:n.330G>T
ENST00000260682.6:c.177G>T ENSP00000260682.6:p.Lys59Asn
ENST00000461906.1:n.202G>T
NM_000771.3:c.177G>T NP_000762.2:p.Lys59Asn
NM_000771.4:c.177G>T MANE Select NP_000762.2:p.Lys59Asn