Canonical Allele Identifier: CA211731651

Gene: CYP2C8

Linked Data

• dbSNP Id: rs371907206
• gnomAD v3: 10-95068591-A-G
• gnomAD v4: 10-95068591-A-G
• MyVariant Identifiers: chr10:g.96828348A>G (hg19) ; chr10:g.95068591A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95068591A>G , CM000672.2:g.95068591A>G	GRCh38
NC_000010.10:g.96828348A>G , CM000672.1:g.96828348A>G	GRCh37
NC_000010.9:g.96818338A>G	NCBI36
NG_007972.1:g.5907T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.168+644T>C MANE Select	ENSP00000360317.3:n.168+644T>C
ENST00000371270.5:c.168+644T>C	ENSP00000360317.3:n.168+644T>C
ENST00000479946.2:n.301+606T>C
ENST00000490994.6:c.206+606T>C	ENSP00000433314.1:n.206+606T>C
ENST00000525991.5:c.206+606T>C	ENSP00000433842.1:n.206+606T>C
ENST00000526814.5:n.252+644T>C
ENST00000527420.5:c.168+644T>C	ENSP00000433191.1:n.168+644T>C
ENST00000527953.5:n.252+644T>C
ENST00000533320.5:n.231+606T>C
ENST00000535898.5:c.25+606T>C	ENSP00000445062.1:n.25+606T>C
ENST00000539050.5:c.-67T>C	ENSP00000442343.2:n.-67T>C
ENST00000623108.3:c.-43+606T>C	ENSP00000485110.1:n.-43+606T>C
NM_000770.3:c.168+644T>C MANE Select	NP_000761.3:n.168+644T>C
NM_001198853.1:c.-43+606T>C	NP_001185782.1:n.-43+606T>C
NM_001198854.1:c.25+606T>C	NP_001185783.1:n.25+606T>C
NM_001198855.1:c.-67T>C	NP_001185784.1:n.-67T>C
XR_945610.1:n.264+644T>C