Canonical Allele Identifier: CA346066958

Gene: POMC

Linked Data

• gnomAD v4: 2-25161400-T-G
• MyVariant Identifiers: chr2:g.25384269T>G (hg19) ; chr2:g.25161400T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25161400T>G , CM000664.2:g.25161400T>G	GRCh38
NC_000002.11:g.25384269T>G , CM000664.1:g.25384269T>G	GRCh37
NC_000002.10:g.25237773T>G	NCBI36
NG_008997.1:g.12291A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395826.7:c.485A>C MANE Select	ENSP00000379170.2:p.Asn162Thr
ENST00000264708.7:c.485A>C	ENSP00000264708.3:p.Asn162Thr
ENST00000380794.5:c.485A>C	ENSP00000370171.1:p.Asn162Thr
ENST00000395826.6:c.485A>C	ENSP00000379170.2:p.Asn162Thr
ENST00000405623.5:c.485A>C	ENSP00000384092.1:p.Asn162Thr
ENST00000449220.1:c.485A>C	ENSP00000387993.1:p.Asn162Thr
NM_000939.2:c.485A>C	NP_000930.1:p.Asn162Thr
NM_001035256.1:c.485A>C	NP_001030333.1:p.Asn162Thr
XM_011532917.1:c.485A>C	XP_011531219.1:p.Asn162Thr
NM_000939.3:c.485A>C	NP_000930.1:p.Asn162Thr
NM_001035256.2:c.485A>C	NP_001030333.1:p.Asn162Thr
NM_001319204.1:c.485A>C	NP_001306133.1:p.Asn162Thr
NM_001319205.1:c.485A>C	NP_001306134.1:p.Asn162Thr
NM_000939.4:c.485A>C MANE Select	NP_000930.1:p.Asn162Thr
NM_001319204.2:c.485A>C	NP_001306133.1:p.Asn162Thr
NM_001319205.2:c.485A>C	NP_001306134.1:p.Asn162Thr
NM_001035256.3:c.485A>C	NP_001030333.1:p.Asn162Thr