Canonical Allele Identifier: CA5617428
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs775537358

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989052T>C , CM000672.2:g.94989052T>C GRCh38
NC_000010.10:g.96748809T>C , CM000672.1:g.96748809T>C GRCh37
NC_000010.9:g.96738799T>C NCBI36
NG_008385.1:g.55395T>C
NG_008385.2:g.55895T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.*24T>C MANE Select ENSP00000260682.6:n.*24T>C
ENST00000643112.1:c.*506T>C ENSP00000496202.1:n.*506T>C
ENST00000260682.6:c.*24T>C ENSP00000260682.6:n.*24T>C
NM_000771.3:c.*24T>C NP_000762.2:n.*24T>C
NM_000771.4:c.*24T>C MANE Select NP_000762.2:n.*24T>C