Canonical Allele Identifier: CA1146937370
Gene: CPT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53196695G= , CM000663.2:g.53196695G= GRCh38
NC_000001.10:g.53662367G= , CM000663.1:g.53662367G= GRCh37
NC_000001.9:g.53434955G= NCBI36
NG_008035.1:g.5267G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371486.3:c.-249G= ENSP00000360541.3:n.-249G=
NM_000098.2:c.-249G= NP_000089.1:n.-249G=
NM_001330589.1:c.-249G= NP_001317518.1:n.-249G=