Canonical Allele Identifier: CA5617507

Gene: CYP2C8

Linked Data

• dbSNP Id: rs755108098
• ExAC: 10:96798649 A / G
• gnomAD v2: 10-96798649-A-G
• gnomAD v3: 10-95038892-A-G
• gnomAD v4: 10-95038892-A-G
• MyVariant Identifiers: chr10:g.96798649A>G (hg19) ; chr10:g.95038892A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95038892A>G , CM000672.2:g.95038892A>G	GRCh38
NC_000010.10:g.96798649A>G , CM000672.1:g.96798649A>G	GRCh37
NC_000010.9:g.96788639A>G	NCBI36
NG_007972.1:g.35606T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371270.6:c.1291+5T>C MANE Select	ENSP00000360317.3:n.1291+5T>C
ENST00000371270.5:c.1291+5T>C	ENSP00000360317.3:n.1291+5T>C
ENST00000490994.6:c.*1077+5T>C	ENSP00000433314.1:n.*1077+5T>C
ENST00000525991.5:c.*866+5T>C	ENSP00000433842.1:n.*866+5T>C
ENST00000526814.5:n.1546+5T>C
ENST00000527420.5:c.*148+5T>C	ENSP00000433191.1:n.*148+5T>C
ENST00000527953.5:n.1585+5T>C
ENST00000531714.1:n.479+5T>C
ENST00000533320.5:n.1525+5T>C
ENST00000535898.5:c.985+5T>C	ENSP00000445062.1:n.985+5T>C
ENST00000539050.5:c.1081+5T>C	ENSP00000442343.2:n.1081+5T>C
ENST00000623108.3:c.1081+5T>C	ENSP00000485110.1:n.1081+5T>C
NM_000770.3:c.1291+5T>C MANE Select	NP_000761.3:n.1291+5T>C
NM_001198853.1:c.1081+5T>C	NP_001185782.1:n.1081+5T>C
NM_001198854.1:c.985+5T>C	NP_001185783.1:n.985+5T>C
NM_001198855.1:c.1081+5T>C	NP_001185784.1:n.1081+5T>C
XR_945610.1:n.1426+5T>C