Canonical Allele Identifier: CA43684210

Gene: POMC

Linked Data

• dbSNP Id: rs774779177
• gnomAD v4: 2-25161048-G-A
• MyVariant Identifiers: chr2:g.25161048G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25161048G>A , CM000664.2:g.25161048G>A	GRCh38
NC_000002.11:g.25383917G>A , CM000664.1:g.25383917G>A	GRCh37
NC_000002.10:g.25237421G>A	NCBI36
NG_008997.1:g.12643C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395826.7:c.*33C>T MANE Select	ENSP00000379170.2:n.*33C>T
ENST00000264708.7:c.*33C>T	ENSP00000264708.3:n.*33C>T
ENST00000380794.5:c.*33C>T	ENSP00000370171.1:n.*33C>T
ENST00000405623.5:c.*33C>T	ENSP00000384092.1:n.*33C>T
NM_000939.2:c.*33C>T	NP_000930.1:n.*33C>T
NM_001035256.1:c.*33C>T	NP_001030333.1:n.*33C>T
XM_011532917.1:c.*33C>T	XP_011531219.1:n.*33C>T
NM_000939.3:c.*33C>T	NP_000930.1:n.*33C>T
NM_001035256.2:c.*33C>T	NP_001030333.1:n.*33C>T
NM_001319204.1:c.*33C>T	NP_001306133.1:n.*33C>T
NM_001319205.1:c.*33C>T	NP_001306134.1:n.*33C>T
NM_000939.4:c.*33C>T MANE Select	NP_000930.1:n.*33C>T
NM_001319204.2:c.*33C>T	NP_001306133.1:n.*33C>T
NM_001319205.2:c.*33C>T	NP_001306134.1:n.*33C>T
NM_001035256.3:c.*33C>T	NP_001030333.1:n.*33C>T