Canonical Allele Identifier: CA43684818

Gene: POMC

Linked Data

• ClinVar Variation Id: 3058717
• ClinVar RCV Id: RCV004542508
• dbSNP Id: rs1020449183
• gnomAD v2: 2-25384442-G-A
• gnomAD v3: 2-25161573-G-A
• gnomAD v4: 2-25161573-G-A
• MyVariant Identifiers: chr2:g.25384442G>A (hg19) ; chr2:g.25161573G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25161573G>A , CM000664.2:g.25161573G>A	GRCh38
NC_000002.11:g.25384442G>A , CM000664.1:g.25384442G>A	GRCh37
NC_000002.10:g.25237946G>A	NCBI36
NG_008997.1:g.12118C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395826.7:c.312C>T MANE Select	ENSP00000379170.2:p.Arg104=
ENST00000264708.7:c.312C>T	ENSP00000264708.3:p.Arg104=
ENST00000380794.5:c.312C>T	ENSP00000370171.1:p.Arg104=
ENST00000395826.6:c.312C>T	ENSP00000379170.2:p.Arg104=
ENST00000405623.5:c.312C>T	ENSP00000384092.1:p.Arg104=
ENST00000449220.1:c.312C>T	ENSP00000387993.1:p.Arg104=
NM_000939.2:c.312C>T	NP_000930.1:p.Arg104=
NM_001035256.1:c.312C>T	NP_001030333.1:p.Arg104=
XM_011532917.1:c.312C>T	XP_011531219.1:p.Arg104=
NM_000939.3:c.312C>T	NP_000930.1:p.Arg104=
NM_001035256.2:c.312C>T	NP_001030333.1:p.Arg104=
NM_001319204.1:c.312C>T	NP_001306133.1:p.Arg104=
NM_001319205.1:c.312C>T	NP_001306134.1:p.Arg104=
NM_000939.4:c.312C>T MANE Select	NP_000930.1:p.Arg104=
NM_001319204.2:c.312C>T	NP_001306133.1:p.Arg104=
NM_001319205.2:c.312C>T	NP_001306134.1:p.Arg104=
NM_001035256.3:c.312C>T	NP_001030333.1:p.Arg104=