Canonical Allele Identifier: CA1742314231
Gene: LEP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128241249A= , CM000669.2:g.128241249A= GRCh38
NC_000007.13:g.127881302A= , CM000669.1:g.127881302A= GRCh37
NC_000007.12:g.127668538A= NCBI36
NG_007450.1:g.4972A=

Transcript Alleles

HGVS Amino-acid Change
XM_005250340.3:c.-86A= XP_005250397.1:n.-86A=
XM_005250340.5:c.-86A= XP_005250397.1:n.-86A=