Canonical Allele Identifier: CA2777834625
Gene: LEP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128241220G>C , CM000669.2:g.128241220G>C GRCh38
NC_000007.13:g.127881273G>C , CM000669.1:g.127881273G>C GRCh37
NC_000007.12:g.127668509G>C NCBI36
NG_007450.1:g.4943G>C

Transcript Alleles

HGVS Amino-acid Change
XM_005250340.3:c.-115G>C XP_005250397.1:n.-115G>C
XM_005250340.5:c.-115G>C XP_005250397.1:n.-115G>C