Canonical Allele Identifier: CA425180299
Gene: POMC HGNC NCBI

Linked Data

gnomAD v4: 2-25161738-G-C
MyVariant Identifiers: chr2:g.25384607G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25161738G>C , CM000664.2:g.25161738G>C GRCh38
NC_000002.11:g.25384607G>C , CM000664.1:g.25384607G>C GRCh37
NC_000002.10:g.25238111G>C NCBI36
NG_008997.1:g.11953C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000395826.7:c.147C>G MANE Select ENSP00000379170.2:p.Ala49=
ENST00000264708.7:c.147C>G ENSP00000264708.3:p.Ala49=
ENST00000380794.5:c.147C>G ENSP00000370171.1:p.Ala49=
ENST00000395826.6:c.147C>G ENSP00000379170.2:p.Ala49=
ENST00000405623.5:c.147C>G ENSP00000384092.1:p.Ala49=
ENST00000449220.1:c.147C>G ENSP00000387993.1:p.Ala49=
NM_000939.2:c.147C>G NP_000930.1:p.Ala49=
NM_001035256.1:c.147C>G NP_001030333.1:p.Ala49=
XM_011532917.1:c.147C>G XP_011531219.1:p.Ala49=
NM_000939.3:c.147C>G NP_000930.1:p.Ala49=
NM_001035256.2:c.147C>G NP_001030333.1:p.Ala49=
NM_001319204.1:c.147C>G NP_001306133.1:p.Ala49=
NM_001319205.1:c.147C>G NP_001306134.1:p.Ala49=
NM_000939.4:c.147C>G MANE Select NP_000930.1:p.Ala49=
NM_001319204.2:c.147C>G NP_001306133.1:p.Ala49=
NM_001319205.2:c.147C>G NP_001306134.1:p.Ala49=
NM_001035256.3:c.147C>G NP_001030333.1:p.Ala49=