Canonical Allele Identifier: CA211730516

Gene: CYP2C8

Linked Data

• dbSNP Id: rs962133452
• MyVariant Identifiers: chr10:g.96826964del (hg19) ; chr10:g.95067207del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067209del , CM000672.2:g.95067209del	GRCh38
NC_000010.10:g.96826966del , CM000672.1:g.96826966del	GRCh37
NC_000010.9:g.96816956del	NCBI36
NG_007972.1:g.7291del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.481+1del
ENST00000371270.5:c.481+1del
ENST00000479946.2:n.785+1del
ENST00000490994.6:c.*267+1del
ENST00000525991.5:c.*56+1del
ENST00000526814.5:n.736+1del
ENST00000527420.5:c.481+1del
ENST00000527953.5:n.736+1del
ENST00000533320.5:n.715+1del
ENST00000535898.5:c.175+1del
ENST00000539050.5:c.271+1del
ENST00000623108.3:c.271+1del
ENST00000628935.1:c.223+1del
NM_000770.3:c.481+1del
NM_001198853.1:c.271+1del
NM_001198854.1:c.175+1del
NM_001198855.1:c.271+1del
XR_945610.1:n.577+1del