Canonical Allele Identifier: CA377677460

Gene: CYP2C8

Linked Data

• dbSNP Id: rs2032902544
• gnomAD v3: 10-95037238-T-G
• gnomAD v4: 10-95037238-T-G
• MyVariant Identifiers: chr10:g.96796995T>G (hg19) ; chr10:g.95037238T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037238T>G , CM000672.2:g.95037238T>G	GRCh38
NC_000010.10:g.96796995T>G , CM000672.1:g.96796995T>G	GRCh37
NC_000010.9:g.96786985T>G	NCBI36
NG_007972.1:g.37260A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1363A>C MANE Select	ENSP00000360317.3:p.Asn455His
ENST00000371270.5:c.1363A>C	ENSP00000360317.3:p.Asn455His
ENST00000490994.6:c.*1149A>C	ENSP00000433314.1:n.*1149A>C
ENST00000525991.5:c.*938A>C	ENSP00000433842.1:n.*938A>C
ENST00000526814.5:n.1618A>C
ENST00000527420.5:c.*220A>C	ENSP00000433191.1:n.*220A>C
ENST00000527953.5:n.1657A>C
ENST00000531714.1:n.551A>C
ENST00000533320.5:n.1597A>C
ENST00000535898.5:c.1057A>C	ENSP00000445062.1:p.Asn353His
ENST00000539050.5:c.1153A>C	ENSP00000442343.2:p.Asn385His
ENST00000623108.3:c.1153A>C	ENSP00000485110.1:p.Asn385His
NM_000770.3:c.1363A>C MANE Select	NP_000761.3:p.Asn455His
NM_001198853.1:c.1153A>C	NP_001185782.1:p.Asn385His
NM_001198854.1:c.1057A>C	NP_001185783.1:p.Asn353His
NM_001198855.1:c.1153A>C	NP_001185784.1:p.Asn385His
XR_945610.1:n.1498A>C