Canonical Allele Identifier: CA833089101
Gene: LEP HGNC NCBI

Linked Data

dbSNP Id: rs1050634161
gnomAD v4: 7-128241207-C-A
MyVariant Identifiers: chr7:g.127881260C>A (hg19) chr7:g.128241207C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128241207C>A , CM000669.2:g.128241207C>A GRCh38
NC_000007.13:g.127881260C>A , CM000669.1:g.127881260C>A GRCh37
NC_000007.12:g.127668496C>A NCBI36
NG_007450.1:g.4930C>A

Transcript Alleles

HGVS Amino-acid Change
XM_005250340.3:c.-128C>A XP_005250397.1:n.-128C>A
XM_005250340.5:c.-128C>A XP_005250397.1:n.-128C>A
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