Canonical Allele Identifier: CA833092144
Gene: LEP HGNC NCBI

Linked Data

dbSNP Id: rs1158694955
gnomAD v3: 7-128247417-C-G
gnomAD v4: 7-128247417-C-G
MyVariant Identifiers: chr7:g.127887470C>G (hg19) chr7:g.128247417C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128247417C>G , CM000669.2:g.128247417C>G GRCh38
NC_000007.13:g.127887470C>G , CM000669.1:g.127887470C>G GRCh37
NC_000007.12:g.127674706C>G NCBI36
NG_007450.1:g.11140C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000308868.5:c.-28-4574C>G MANE Select ENSP00000312652.4:n.-28-4574C>G
ENST00000308868.4:c.-28-4574C>G ENSP00000312652.4:n.-28-4574C>G
NM_000230.2:c.-28-4574C>G NP_000221.1:n.-28-4574C>G
XM_005250340.3:c.-28-4574C>G XP_005250397.1:n.-28-4574C>G
XM_005250340.5:c.-28-4574C>G XP_005250397.1:n.-28-4574C>G
NM_000230.3:c.-28-4574C>G MANE Select NP_000221.1:n.-28-4574C>G
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