Canonical Allele Identifier: CA2743635132
Gene: CPT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53196766A>G , CM000663.2:g.53196766A>G GRCh38
NC_000001.10:g.53662438A>G , CM000663.1:g.53662438A>G GRCh37
NC_000001.9:g.53435026A>G NCBI36
NG_008035.1:g.5338A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371486.3:c.-178A>G ENSP00000360541.3:n.-178A>G
NM_000098.2:c.-178A>G NP_000089.1:n.-178A>G
XM_005270484.1:c.-178A>G XP_005270541.1:n.-178A>G
NM_001330589.1:c.-178A>G NP_001317518.1:n.-178A>G