Canonical Allele Identifier: CA2645706447
Gene: CPT2 HGNC NCBI

Linked Data

gnomAD v4: 1-53196783-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53196783G>A , CM000663.2:g.53196783G>A GRCh38
NC_000001.10:g.53662455G>A , CM000663.1:g.53662455G>A GRCh37
NC_000001.9:g.53435043G>A NCBI36
NG_008035.1:g.5355G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371486.3:c.-161G>A ENSP00000360541.3:n.-161G>A
NM_000098.2:c.-161G>A NP_000089.1:n.-161G>A
XM_005270484.1:c.-161G>A XP_005270541.1:n.-161G>A
NM_001330589.1:c.-161G>A NP_001317518.1:n.-161G>A
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