Canonical Allele Identifier: CA425352835

Gene: POMC

Linked Data

• MyVariant Identifiers: chr2:g.25383968G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25161099G>C , CM000664.2:g.25161099G>C	GRCh38
NC_000002.11:g.25383968G>C , CM000664.1:g.25383968G>C	GRCh37
NC_000002.10:g.25237472G>C	NCBI36
NG_008997.1:g.12592C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000395826.7:c.786C>G MANE Select	ENSP00000379170.2:p.Ala262=
ENST00000264708.7:c.786C>G	ENSP00000264708.3:p.Ala262=
ENST00000380794.5:c.786C>G	ENSP00000370171.1:p.Ala262=
ENST00000395826.6:c.786C>G	ENSP00000379170.2:p.Ala262=
ENST00000405623.5:c.786C>G	ENSP00000384092.1:p.Ala262=
NM_000939.2:c.786C>G	NP_000930.1:p.Ala262=
NM_001035256.1:c.786C>G	NP_001030333.1:p.Ala262=
XM_011532917.1:c.786C>G	XP_011531219.1:p.Ala262=
NM_000939.3:c.786C>G	NP_000930.1:p.Ala262=
NM_001035256.2:c.786C>G	NP_001030333.1:p.Ala262=
NM_001319204.1:c.786C>G	NP_001306133.1:p.Ala262=
NM_001319205.1:c.786C>G	NP_001306134.1:p.Ala262=
NM_000939.4:c.786C>G MANE Select	NP_000930.1:p.Ala262=
NM_001319204.2:c.786C>G	NP_001306133.1:p.Ala262=
NM_001319205.2:c.786C>G	NP_001306134.1:p.Ala262=
NM_001035256.3:c.786C>G	NP_001030333.1:p.Ala262=