Canonical Allele Identifier: CA211731644

Gene: CYP2C8

Linked Data

• dbSNP Id: rs934786692
• gnomAD v4: 10-95068578-T-G
• MyVariant Identifiers: chr10:g.96828335T>G (hg19) ; chr10:g.95068578T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95068578T>G , CM000672.2:g.95068578T>G	GRCh38
NC_000010.10:g.96828335T>G , CM000672.1:g.96828335T>G	GRCh37
NC_000010.9:g.96818325T>G	NCBI36
NG_007972.1:g.5920A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371270.6:c.168+657A>C MANE Select	ENSP00000360317.3:n.168+657A>C
ENST00000371270.5:c.168+657A>C	ENSP00000360317.3:n.168+657A>C
ENST00000479946.2:n.301+619A>C
ENST00000490994.6:c.206+619A>C	ENSP00000433314.1:n.206+619A>C
ENST00000525991.5:c.206+619A>C	ENSP00000433842.1:n.206+619A>C
ENST00000526814.5:n.252+657A>C
ENST00000527420.5:c.168+657A>C	ENSP00000433191.1:n.168+657A>C
ENST00000527953.5:n.252+657A>C
ENST00000533320.5:n.231+619A>C
ENST00000535898.5:c.25+619A>C	ENSP00000445062.1:n.25+619A>C
ENST00000539050.5:c.-54A>C	ENSP00000442343.2:n.-54A>C
ENST00000623108.3:c.-43+619A>C	ENSP00000485110.1:n.-43+619A>C
NM_000770.3:c.168+657A>C MANE Select	NP_000761.3:n.168+657A>C
NM_001198853.1:c.-43+619A>C	NP_001185782.1:n.-43+619A>C
NM_001198854.1:c.25+619A>C	NP_001185783.1:n.25+619A>C
NM_001198855.1:c.-54A>C	NP_001185784.1:n.-54A>C
XR_945610.1:n.264+657A>C