Canonical Allele Identifier: CA377682618

Gene: CYP2C8

Linked Data

• dbSNP Id: rs1419635449
• gnomAD v2: 10-96826972-T-A
• gnomAD v4: 10-95067215-T-A
• MyVariant Identifiers: chr10:g.96826972T>A (hg19) ; chr10:g.95067215T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067215T>A , CM000672.2:g.95067215T>A	GRCh38
NC_000010.10:g.96826972T>A , CM000672.1:g.96826972T>A	GRCh37
NC_000010.9:g.96816962T>A	NCBI36
NG_007972.1:g.7283A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.474A>T MANE Select	ENSP00000360317.3:p.Lys158Asn
ENST00000371270.5:c.474A>T	ENSP00000360317.3:p.Lys158Asn
ENST00000479946.2:n.778A>T
ENST00000490994.6:c.*260A>T	ENSP00000433314.1:n.*260A>T
ENST00000525991.5:c.*49A>T	ENSP00000433842.1:n.*49A>T
ENST00000526814.5:n.729A>T
ENST00000527420.5:c.474A>T	ENSP00000433191.1:p.Lys158Asn
ENST00000527953.5:n.729A>T
ENST00000533320.5:n.708A>T
ENST00000535898.5:c.168A>T	ENSP00000445062.1:p.Lys56Asn
ENST00000539050.5:c.264A>T	ENSP00000442343.2:p.Lys88Asn
ENST00000623108.3:c.264A>T	ENSP00000485110.1:p.Lys88Asn
ENST00000628935.1:c.216A>T	ENSP00000487145.1:p.Lys72Asn
NM_000770.3:c.474A>T MANE Select	NP_000761.3:p.Lys158Asn
NM_001198853.1:c.264A>T	NP_001185782.1:p.Lys88Asn
NM_001198854.1:c.168A>T	NP_001185783.1:p.Lys56Asn
NM_001198855.1:c.264A>T	NP_001185784.1:p.Lys88Asn
XR_945610.1:n.570A>T