Canonical Allele Identifier: CA1167208832
Gene: CPT2 HGNC NCBI

Linked Data

dbSNP Id: rs1645322724
gnomAD v4: 1-53196774-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53196774G>A , CM000663.2:g.53196774G>A GRCh38
NC_000001.10:g.53662446G>A , CM000663.1:g.53662446G>A GRCh37
NC_000001.9:g.53435034G>A NCBI36
NG_008035.1:g.5346G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371486.3:c.-170G>A ENSP00000360541.3:n.-170G>A
NM_000098.2:c.-170G>A NP_000089.1:n.-170G>A
XM_005270484.1:c.-170G>A XP_005270541.1:n.-170G>A
NM_001330589.1:c.-170G>A NP_001317518.1:n.-170G>A