Canonical Allele Identifier: CA377682771

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96826998G>T (hg19) ; chr10:g.95067241G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067241G>T , CM000672.2:g.95067241G>T	GRCh38
NC_000010.10:g.96826998G>T , CM000672.1:g.96826998G>T	GRCh37
NC_000010.9:g.96816988G>T	NCBI36
NG_007972.1:g.7257C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.448C>A MANE Select	ENSP00000360317.3:p.His150Asn
ENST00000371270.5:c.448C>A	ENSP00000360317.3:p.His150Asn
ENST00000479946.2:n.752C>A
ENST00000490994.6:c.*234C>A	ENSP00000433314.1:n.*234C>A
ENST00000525991.5:c.*23C>A	ENSP00000433842.1:n.*23C>A
ENST00000526814.5:n.703C>A
ENST00000527420.5:c.448C>A	ENSP00000433191.1:p.His150Asn
ENST00000527953.5:n.703C>A
ENST00000533320.5:n.682C>A
ENST00000535898.5:c.142C>A	ENSP00000445062.1:p.His48Asn
ENST00000539050.5:c.238C>A	ENSP00000442343.2:p.His80Asn
ENST00000623108.3:c.238C>A	ENSP00000485110.1:p.His80Asn
ENST00000628935.1:c.190C>A	ENSP00000487145.1:p.His64Asn
NM_000770.3:c.448C>A MANE Select	NP_000761.3:p.His150Asn
NM_001198853.1:c.238C>A	NP_001185782.1:p.His80Asn
NM_001198854.1:c.142C>A	NP_001185783.1:p.His48Asn
NM_001198855.1:c.238C>A	NP_001185784.1:p.His80Asn
XR_945610.1:n.544C>A