Canonical Allele Identifier: CA2789072705
Gene: CYP2C9 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942776T>C , CM000672.2:g.94942776T>C GRCh38
NC_000010.10:g.96702533T>C , CM000672.1:g.96702533T>C GRCh37
NC_000010.9:g.96692523T>C NCBI36
NG_008385.1:g.9119T>C
NG_008385.2:g.9619T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.481+435T>C MANE Select ENSP00000260682.6:n.481+435T>C
ENST00000643112.1:c.481+435T>C ENSP00000496202.1:n.481+435T>C
ENST00000645207.1:n.634+435T>C
ENST00000260682.6:c.481+435T>C ENSP00000260682.6:n.481+435T>C
ENST00000461906.1:n.941T>C
ENST00000473496.1:n.252+435T>C
NM_000771.3:c.481+435T>C NP_000762.2:n.481+435T>C
NM_000771.4:c.481+435T>C MANE Select NP_000762.2:n.481+435T>C
Search 100 bp 5'
Search 100 bp 3'