Canonical Allele Identifier: CA1167208732
Gene: CPT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53196647C= , CM000663.2:g.53196647C= GRCh38
NC_000001.10:g.53662319C= , CM000663.1:g.53662319C= GRCh37
NC_000001.9:g.53434907C= NCBI36
NG_008035.1:g.5219C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371486.3:c.-297C= ENSP00000360541.3:n.-297C=
NM_000098.2:c.-297C= NP_000089.1:n.-297C=
NM_001330589.1:c.-297C= NP_001317518.1:n.-297C=