Canonical Allele Identifier: CA2684761948
Gene: LEP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128241248T>C , CM000669.2:g.128241248T>C GRCh38
NC_000007.13:g.127881301T>C , CM000669.1:g.127881301T>C GRCh37
NC_000007.12:g.127668537T>C NCBI36
NG_007450.1:g.4971T>C

Transcript Alleles

HGVS Amino-acid Change
XM_005250340.3:c.-87T>C XP_005250397.1:n.-87T>C
XM_005250340.5:c.-87T>C XP_005250397.1:n.-87T>C