Canonical Allele Identifier: CA1742314213
Gene: LEP HGNC NCBI

Linked Data

dbSNP Id: rs1795145697
gnomAD v4: 7-128241221-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128241221C>T , CM000669.2:g.128241221C>T GRCh38
NC_000007.13:g.127881274C>T , CM000669.1:g.127881274C>T GRCh37
NC_000007.12:g.127668510C>T NCBI36
NG_007450.1:g.4944C>T

Transcript Alleles

HGVS Amino-acid Change
XM_005250340.3:c.-114C>T XP_005250397.1:n.-114C>T
XM_005250340.5:c.-114C>T XP_005250397.1:n.-114C>T
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