Canonical Allele Identifier: CA22626016
Gene: CPT2 HGNC NCBI

Linked Data

dbSNP Id: rs935571143
gnomAD v4: 1-53196679-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53196679G>A , CM000663.2:g.53196679G>A GRCh38
NC_000001.10:g.53662351G>A , CM000663.1:g.53662351G>A GRCh37
NC_000001.9:g.53434939G>A NCBI36
NG_008035.1:g.5251G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371486.3:c.-265G>A ENSP00000360541.3:n.-265G>A
NM_000098.2:c.-265G>A NP_000089.1:n.-265G>A
NM_001330589.1:c.-265G>A NP_001317518.1:n.-265G>A