Canonical Allele Identifier: CA2645706329
Gene: CPT2 HGNC NCBI

Linked Data

gnomAD v4: 1-53196641-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53196641C>A , CM000663.2:g.53196641C>A GRCh38
NC_000001.10:g.53662313C>A , CM000663.1:g.53662313C>A GRCh37
NC_000001.9:g.53434901C>A NCBI36
NG_008035.1:g.5213C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371486.3:c.-303C>A ENSP00000360541.3:n.-303C>A
NM_000098.2:c.-303C>A NP_000089.1:n.-303C>A
NM_001330589.1:c.-303C>A NP_001317518.1:n.-303C>A