Canonical Allele Identifier: CA166743867
Gene: LEP HGNC NCBI

Linked Data

dbSNP Id: rs1018091320
MyVariant Identifiers: chr7:g.128248584A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128248584A>T , CM000669.2:g.128248584A>T GRCh38
NC_000007.13:g.127888637A>T , CM000669.1:g.127888637A>T GRCh37
NC_000007.12:g.127675873A>T NCBI36
NG_007450.1:g.12307A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000308868.5:c.-28-3407A>T MANE Select ENSP00000312652.4:n.-28-3407A>T
ENST00000308868.4:c.-28-3407A>T ENSP00000312652.4:n.-28-3407A>T
NM_000230.2:c.-28-3407A>T NP_000221.1:n.-28-3407A>T
XM_005250340.3:c.-28-3407A>T XP_005250397.1:n.-28-3407A>T
XM_005250340.5:c.-28-3407A>T XP_005250397.1:n.-28-3407A>T
NM_000230.3:c.-28-3407A>T MANE Select NP_000221.1:n.-28-3407A>T
Search 100 bp 5'
Search 100 bp 3'