Canonical Allele Identifier: CA736875906
Gene: CPT2 HGNC NCBI

Linked Data

dbSNP Id: rs1193473316
gnomAD v4: 1-53196759-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53196759G>T , CM000663.2:g.53196759G>T GRCh38
NC_000001.10:g.53662431G>T , CM000663.1:g.53662431G>T GRCh37
NC_000001.9:g.53435019G>T NCBI36
NG_008035.1:g.5331G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371486.3:c.-185G>T ENSP00000360541.3:n.-185G>T
NM_000098.2:c.-185G>T NP_000089.1:n.-185G>T
NM_001330589.1:c.-185G>T NP_001317518.1:n.-185G>T