Canonical Allele Identifier: CA5617776

Gene: CYP2C8

Linked Data

• dbSNP Id: rs747268921
• ExAC: 10:96826944 A / G
• gnomAD v2: 10-96826944-A-G
• gnomAD v4: 10-95067187-A-G
• MyVariant Identifiers: chr10:g.96826944A>G (hg19) ; chr10:g.95067187A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067187A>G , CM000672.2:g.95067187A>G	GRCh38
NC_000010.10:g.96826944A>G , CM000672.1:g.96826944A>G	GRCh37
NC_000010.9:g.96816934A>G	NCBI36
NG_007972.1:g.7311T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.481+21T>C MANE Select	ENSP00000360317.3:n.481+21T>C
ENST00000371270.5:c.481+21T>C	ENSP00000360317.3:n.481+21T>C
ENST00000479946.2:n.785+21T>C
ENST00000490994.6:c.*267+21T>C	ENSP00000433314.1:n.*267+21T>C
ENST00000525991.5:c.*56+21T>C	ENSP00000433842.1:n.*56+21T>C
ENST00000526814.5:n.736+21T>C
ENST00000527420.5:c.481+21T>C	ENSP00000433191.1:n.481+21T>C
ENST00000527953.5:n.736+21T>C
ENST00000533320.5:n.715+21T>C
ENST00000535898.5:c.175+21T>C	ENSP00000445062.1:n.175+21T>C
ENST00000539050.5:c.271+21T>C	ENSP00000442343.2:n.271+21T>C
ENST00000623108.3:c.271+21T>C	ENSP00000485110.1:n.271+21T>C
ENST00000628935.1:c.223+21T>C	ENSP00000487145.1:n.223+21T>C
NM_000770.3:c.481+21T>C MANE Select	NP_000761.3:n.481+21T>C
NM_001198853.1:c.271+21T>C	NP_001185782.1:n.271+21T>C
NM_001198854.1:c.175+21T>C	NP_001185783.1:n.175+21T>C
NM_001198855.1:c.271+21T>C	NP_001185784.1:n.271+21T>C
XR_945610.1:n.577+21T>C