Canonical Allele Identifier: CA211693237
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs928126083

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942095C>T , CM000672.2:g.94942095C>T GRCh38
NC_000010.10:g.96701852C>T , CM000672.1:g.96701852C>T GRCh37
NC_000010.9:g.96691842C>T NCBI36
NG_008385.1:g.8438C>T
NG_008385.2:g.8938C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.331+75C>T MANE Select ENSP00000260682.6:n.331+75C>T
ENST00000643112.1:c.331+75C>T ENSP00000496202.1:n.331+75C>T
ENST00000645207.1:n.484+75C>T
ENST00000260682.6:c.331+75C>T ENSP00000260682.6:n.331+75C>T
ENST00000461906.1:n.356+75C>T
ENST00000473496.1:n.102+75C>T
NM_000771.3:c.331+75C>T NP_000762.2:n.331+75C>T
NM_000771.4:c.331+75C>T MANE Select NP_000762.2:n.331+75C>T