Canonical Allele Identifier: CA166742042
Gene: LEP HGNC NCBI

Linked Data

dbSNP Id: rs560478489
gnomAD v3: 7-128241219-G-T
gnomAD v4: 7-128241219-G-T
MyVariant Identifiers: chr7:g.127881272G>T (hg19) chr7:g.128241219G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128241219G>T , CM000669.2:g.128241219G>T GRCh38
NC_000007.13:g.127881272G>T , CM000669.1:g.127881272G>T GRCh37
NC_000007.12:g.127668508G>T NCBI36
NG_007450.1:g.4942G>T

Transcript Alleles

HGVS Amino-acid Change
XM_005250340.3:c.-116G>T XP_005250397.1:n.-116G>T
XM_005250340.5:c.-116G>T XP_005250397.1:n.-116G>T
Search 100 bp 5'
Search 100 bp 3'