Canonical Allele Identifier: CA833092156
Gene: LEP HGNC NCBI

Linked Data

dbSNP Id: rs1267969456
gnomAD v3: 7-128247464-A-G
gnomAD v4: 7-128247464-A-G
MyVariant Identifiers: chr7:g.127887517A>G (hg19) chr7:g.128247464A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128247464A>G , CM000669.2:g.128247464A>G GRCh38
NC_000007.13:g.127887517A>G , CM000669.1:g.127887517A>G GRCh37
NC_000007.12:g.127674753A>G NCBI36
NG_007450.1:g.11187A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000308868.5:c.-28-4527A>G MANE Select ENSP00000312652.4:n.-28-4527A>G
ENST00000308868.4:c.-28-4527A>G ENSP00000312652.4:n.-28-4527A>G
NM_000230.2:c.-28-4527A>G NP_000221.1:n.-28-4527A>G
XM_005250340.3:c.-28-4527A>G XP_005250397.1:n.-28-4527A>G
XM_005250340.5:c.-28-4527A>G XP_005250397.1:n.-28-4527A>G
NM_000230.3:c.-28-4527A>G MANE Select NP_000221.1:n.-28-4527A>G
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