Canonical Allele Identifier: CA123053
Gene: POMC HGNC NCBI

Linked Data

ClinVar Variation Id: 13356
dbSNP Id: rs28932472

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25161179G>C , CM000664.2:g.25161179G>C GRCh38
NC_000002.11:g.25384048G>C , CM000664.1:g.25384048G>C GRCh37
NC_000002.10:g.25237552G>C NCBI36
NG_008997.1:g.12512C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000395826.7:c.706C>G MANE Select ENSP00000379170.2:p.Arg236Gly
ENST00000264708.7:c.706C>G ENSP00000264708.3:p.Arg236Gly
ENST00000380794.5:c.706C>G ENSP00000370171.1:p.Arg236Gly
ENST00000395826.6:c.706C>G ENSP00000379170.2:p.Arg236Gly
ENST00000405623.5:c.706C>G ENSP00000384092.1:p.Arg236Gly
ENST00000449220.1:c.706C>G ENSP00000387993.1:p.Arg236Gly
NM_000939.2:c.706C>G NP_000930.1:p.Arg236Gly
NM_001035256.1:c.706C>G NP_001030333.1:p.Arg236Gly
XM_011532917.1:c.706C>G XP_011531219.1:p.Arg236Gly
NM_000939.3:c.706C>G NP_000930.1:p.Arg236Gly
NM_001035256.2:c.706C>G NP_001030333.1:p.Arg236Gly
NM_001319204.1:c.706C>G NP_001306133.1:p.Arg236Gly
NM_001319205.1:c.706C>G NP_001306134.1:p.Arg236Gly
NM_000939.4:c.706C>G MANE Select NP_000930.1:p.Arg236Gly
NM_001319204.2:c.706C>G NP_001306133.1:p.Arg236Gly
NM_001319205.2:c.706C>G NP_001306134.1:p.Arg236Gly
NM_001035256.3:c.706C>G NP_001030333.1:p.Arg236Gly