Canonical Allele Identifier: CA377677428

Gene: CYP2C8

Linked Data

• dbSNP Id: rs1384731839
• gnomAD v2: 10-96796982-T-G
• gnomAD v4: 10-95037225-T-G
• MyVariant Identifiers: chr10:g.96796982T>G (hg19) ; chr10:g.95037225T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037225T>G , CM000672.2:g.95037225T>G	GRCh38
NC_000010.10:g.96796982T>G , CM000672.1:g.96796982T>G	GRCh37
NC_000010.9:g.96786972T>G	NCBI36
NG_007972.1:g.37273A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1376A>C MANE Select	ENSP00000360317.3:p.Lys459Thr
ENST00000371270.5:c.1376A>C	ENSP00000360317.3:p.Lys459Thr
ENST00000490994.6:c.*1162A>C	ENSP00000433314.1:n.*1162A>C
ENST00000525991.5:c.*951A>C	ENSP00000433842.1:n.*951A>C
ENST00000526814.5:n.1631A>C
ENST00000527420.5:c.*233A>C	ENSP00000433191.1:n.*233A>C
ENST00000527953.5:n.1670A>C
ENST00000531714.1:n.564A>C
ENST00000533320.5:n.1610A>C
ENST00000535898.5:c.1070A>C	ENSP00000445062.1:p.Lys357Thr
ENST00000539050.5:c.1166A>C	ENSP00000442343.2:p.Lys389Thr
ENST00000623108.3:c.1166A>C	ENSP00000485110.1:p.Lys389Thr
NM_000770.3:c.1376A>C MANE Select	NP_000761.3:p.Lys459Thr
NM_001198853.1:c.1166A>C	NP_001185782.1:p.Lys389Thr
NM_001198854.1:c.1070A>C	NP_001185783.1:p.Lys357Thr
NM_001198855.1:c.1166A>C	NP_001185784.1:p.Lys389Thr
XR_945610.1:n.1511A>C