Canonical Allele Identifier: CA2645706350
Gene: CPT2 HGNC NCBI

Linked Data

gnomAD v4: 1-53196670-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53196670G>C , CM000663.2:g.53196670G>C GRCh38
NC_000001.10:g.53662342G>C , CM000663.1:g.53662342G>C GRCh37
NC_000001.9:g.53434930G>C NCBI36
NG_008035.1:g.5242G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371486.3:c.-274G>C ENSP00000360541.3:n.-274G>C
NM_000098.2:c.-274G>C NP_000089.1:n.-274G>C
NM_001330589.1:c.-274G>C NP_001317518.1:n.-274G>C
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