Canonical Allele Identifier: CA1028508008
Gene: POMC HGNC NCBI

Linked Data

dbSNP Id: rs1671625052
gnomAD v3: 2-25168262-A-T
gnomAD v4: 2-25168262-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25168262A>T , CM000664.2:g.25168262A>T GRCh38
NC_000002.11:g.25391131A>T , CM000664.1:g.25391131A>T GRCh37
NC_000002.10:g.25244635A>T NCBI36
NG_008997.1:g.5429T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000395826.7:c.-21+236T>A MANE Select ENSP00000379170.2:n.-21+236T>A
ENST00000264708.7:c.-101+236T>A ENSP00000264708.3:n.-101+236T>A
ENST00000380794.5:c.-71+236T>A ENSP00000370171.1:n.-71+236T>A
ENST00000395826.6:c.-21+236T>A ENSP00000379170.2:n.-21+236T>A
ENST00000405623.5:c.-51+236T>A ENSP00000384092.1:n.-51+236T>A
ENST00000449220.1:c.-71+236T>A ENSP00000387993.1:n.-71+236T>A
NM_000939.2:c.-21+236T>A NP_000930.1:n.-21+236T>A
NM_001035256.1:c.-71+236T>A NP_001030333.1:n.-71+236T>A
XM_011532917.1:c.-51+236T>A XP_011531219.1:n.-51+236T>A
NM_000939.3:c.-21+236T>A NP_000930.1:n.-21+236T>A
NM_001035256.2:c.-71+236T>A NP_001030333.1:n.-71+236T>A
NM_001319204.1:c.-101+236T>A NP_001306133.1:n.-101+236T>A
NM_001319205.1:c.-51+236T>A NP_001306134.1:n.-51+236T>A
NM_000939.4:c.-21+236T>A MANE Select NP_000930.1:n.-21+236T>A
NM_001319204.2:c.-101+236T>A NP_001306133.1:n.-101+236T>A
NM_001319205.2:c.-51+236T>A NP_001306134.1:n.-51+236T>A
NM_001035256.3:c.-71+236T>A NP_001030333.1:n.-71+236T>A