Canonical Allele Identifier: CA166742045
Gene: LEP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128241246G>A , CM000669.2:g.128241246G>A GRCh38
NC_000007.13:g.127881299G>A , CM000669.1:g.127881299G>A GRCh37
NC_000007.12:g.127668535G>A NCBI36
NG_007450.1:g.4969G>A

Transcript Alleles

HGVS Amino-acid Change
XM_005250340.3:c.-89G>A XP_005250397.1:n.-89G>A
XM_005250340.5:c.-89G>A XP_005250397.1:n.-89G>A
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