Canonical Allele Identifier: CA2743635129
Gene: CPT2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53196712C>A , CM000663.2:g.53196712C>A GRCh38
NC_000001.10:g.53662384C>A , CM000663.1:g.53662384C>A GRCh37
NC_000001.9:g.53434972C>A NCBI36
NG_008035.1:g.5284C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371486.3:c.-232C>A ENSP00000360541.3:n.-232C>A
NM_000098.2:c.-232C>A NP_000089.1:n.-232C>A
NM_001330589.1:c.-232C>A NP_001317518.1:n.-232C>A
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