Canonical Allele Identifier: CA2645706287
Gene: CPT2 HGNC NCBI

Linked Data

gnomAD v4: 1-53196604-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53196604C>T , CM000663.2:g.53196604C>T GRCh38
NC_000001.10:g.53662276C>T , CM000663.1:g.53662276C>T GRCh37
NC_000001.9:g.53434864C>T NCBI36
NG_008035.1:g.5176C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371486.3:c.-340C>T ENSP00000360541.3:n.-340C>T
NM_000098.2:c.-340C>T NP_000089.1:n.-340C>T
NM_001330589.1:c.-340C>T NP_001317518.1:n.-340C>T