Canonical Allele Identifier: CA2645706415
Gene: CPT2 HGNC NCBI

Linked Data

gnomAD v4: 1-53196745-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53196745A>C , CM000663.2:g.53196745A>C GRCh38
NC_000001.10:g.53662417A>C , CM000663.1:g.53662417A>C GRCh37
NC_000001.9:g.53435005A>C NCBI36
NG_008035.1:g.5317A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371486.3:c.-199A>C ENSP00000360541.3:n.-199A>C
NM_000098.2:c.-199A>C NP_000089.1:n.-199A>C
NM_001330589.1:c.-199A>C NP_001317518.1:n.-199A>C