Canonical Allele Identifier: CA346067299
Gene: POMC HGNC NCBI

Linked Data

dbSNP Id: rs1395733145
gnomAD v2: 2-25384428-G-C
gnomAD v4: 2-25161559-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25161559G>C , CM000664.2:g.25161559G>C GRCh38
NC_000002.11:g.25384428G>C , CM000664.1:g.25384428G>C GRCh37
NC_000002.10:g.25237932G>C NCBI36
NG_008997.1:g.12132C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000395826.7:c.326C>G MANE Select ENSP00000379170.2:p.Ala109Gly
ENST00000264708.7:c.326C>G ENSP00000264708.3:p.Ala109Gly
ENST00000380794.5:c.326C>G ENSP00000370171.1:p.Ala109Gly
ENST00000395826.6:c.326C>G ENSP00000379170.2:p.Ala109Gly
ENST00000405623.5:c.326C>G ENSP00000384092.1:p.Ala109Gly
ENST00000449220.1:c.326C>G ENSP00000387993.1:p.Ala109Gly
NM_000939.2:c.326C>G NP_000930.1:p.Ala109Gly
NM_001035256.1:c.326C>G NP_001030333.1:p.Ala109Gly
XM_011532917.1:c.326C>G XP_011531219.1:p.Ala109Gly
NM_000939.3:c.326C>G NP_000930.1:p.Ala109Gly
NM_001035256.2:c.326C>G NP_001030333.1:p.Ala109Gly
NM_001319204.1:c.326C>G NP_001306133.1:p.Ala109Gly
NM_001319205.1:c.326C>G NP_001306134.1:p.Ala109Gly
NM_000939.4:c.326C>G MANE Select NP_000930.1:p.Ala109Gly
NM_001319204.2:c.326C>G NP_001306133.1:p.Ala109Gly
NM_001319205.2:c.326C>G NP_001306134.1:p.Ala109Gly
NM_001035256.3:c.326C>G NP_001030333.1:p.Ala109Gly