Canonical Allele Identifier: CA1167208821
Gene: CPT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53196762C= , CM000663.2:g.53196762C= GRCh38
NC_000001.10:g.53662434C= , CM000663.1:g.53662434C= GRCh37
NC_000001.9:g.53435022C= NCBI36
NG_008035.1:g.5334C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371486.3:c.-182C= ENSP00000360541.3:n.-182C=
NM_000098.2:c.-182C= NP_000089.1:n.-182C=
XM_005270484.1:c.-182C= XP_005270541.1:n.-182C=
NM_001330589.1:c.-182C= NP_001317518.1:n.-182C=