Canonical Allele Identifier: CA736875819
Gene: CPT2 HGNC NCBI

Linked Data

dbSNP Id: rs1448651916
gnomAD v4: 1-53196685-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53196685G>A , CM000663.2:g.53196685G>A GRCh38
NC_000001.10:g.53662357G>A , CM000663.1:g.53662357G>A GRCh37
NC_000001.9:g.53434945G>A NCBI36
NG_008035.1:g.5257G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371486.3:c.-259G>A ENSP00000360541.3:n.-259G>A
NM_000098.2:c.-259G>A NP_000089.1:n.-259G>A
NM_001330589.1:c.-259G>A NP_001317518.1:n.-259G>A