Canonical Allele Identifier: CA43684236

Gene: POMC

Linked Data

• dbSNP Id: rs369203419
• gnomAD v3: 2-25161056-G-C
• gnomAD v4: 2-25161056-G-C
• MyVariant Identifiers: chr2:g.25383925G>C (hg19) ; chr2:g.25161056G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25161056G>C , CM000664.2:g.25161056G>C	GRCh38
NC_000002.11:g.25383925G>C , CM000664.1:g.25383925G>C	GRCh37
NC_000002.10:g.25237429G>C	NCBI36
NG_008997.1:g.12635C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395826.7:c.*25C>G MANE Select	ENSP00000379170.2:n.*25C>G
ENST00000264708.7:c.*25C>G	ENSP00000264708.3:n.*25C>G
ENST00000380794.5:c.*25C>G	ENSP00000370171.1:n.*25C>G
ENST00000395826.6:c.*25C>G	ENSP00000379170.2:n.*25C>G
ENST00000405623.5:c.*25C>G	ENSP00000384092.1:n.*25C>G
NM_000939.2:c.*25C>G	NP_000930.1:n.*25C>G
NM_001035256.1:c.*25C>G	NP_001030333.1:n.*25C>G
XM_011532917.1:c.*25C>G	XP_011531219.1:n.*25C>G
NM_000939.3:c.*25C>G	NP_000930.1:n.*25C>G
NM_001035256.2:c.*25C>G	NP_001030333.1:n.*25C>G
NM_001319204.1:c.*25C>G	NP_001306133.1:n.*25C>G
NM_001319205.1:c.*25C>G	NP_001306134.1:n.*25C>G
NM_000939.4:c.*25C>G MANE Select	NP_000930.1:n.*25C>G
NM_001319204.2:c.*25C>G	NP_001306133.1:n.*25C>G
NM_001319205.2:c.*25C>G	NP_001306134.1:n.*25C>G
NM_001035256.3:c.*25C>G	NP_001030333.1:n.*25C>G