Canonical Allele Identifier: CA1167208779
Gene: CPT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53196710T= , CM000663.2:g.53196710T= GRCh38
NC_000001.10:g.53662382T= , CM000663.1:g.53662382T= GRCh37
NC_000001.9:g.53434970T= NCBI36
NG_008035.1:g.5282T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371486.3:c.-234T= ENSP00000360541.3:n.-234T=
NM_000098.2:c.-234T= NP_000089.1:n.-234T=
NM_001330589.1:c.-234T= NP_001317518.1:n.-234T=