Canonical Allele Identifier: CA2645706413
Gene: CPT2 HGNC NCBI

Linked Data

gnomAD v4: 1-53196741-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53196741T>G , CM000663.2:g.53196741T>G GRCh38
NC_000001.10:g.53662413T>G , CM000663.1:g.53662413T>G GRCh37
NC_000001.9:g.53435001T>G NCBI36
NG_008035.1:g.5313T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371486.3:c.-203T>G ENSP00000360541.3:n.-203T>G
NM_000098.2:c.-203T>G NP_000089.1:n.-203T>G
NM_001330589.1:c.-203T>G NP_001317518.1:n.-203T>G