Canonical Allele Identifier: CA15527886
Gene: LEP HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs12706832

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128247086A>G , CM000669.2:g.128247086A>G GRCh38
NC_000007.13:g.127887139A>G , CM000669.1:g.127887139A>G GRCh37
NC_000007.12:g.127674375A>G NCBI36
NG_007450.1:g.10809A>G

Transcript Alleles

HGVS Amino-acid change
NM_000230.2:c.-28-4905A>G VV NP_000221.1:p.=
XM_005250340.3:c.-28-4905A>G XP_005250397.1:p.=
XM_005250340.5:c.-28-4905A>G XP_005250397.1:p.=
NM_000230.3:c.-28-4905A>G VV MANE Preferred NP_000221.1:p.=
ENST00000308868.4:c.-28-4905A>G ENSP00000312652.4:p.=