Canonical Allele Identifier: CA2285919602
Gene: MC2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13885537A= , CM000680.2:g.13885537A= GRCh38
NC_000018.9:g.13885536A= , CM000680.1:g.13885536A= GRCh37
NC_000018.8:g.13875536A= NCBI36
NG_011819.1:g.35000T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327606.4:c.-19T= MANE Select ENSP00000333821.2:n.-19T=
ENST00000327606.3:c.-19T= ENSP00000333821.2:n.-19T=
ENST00000399821.2:c.-19T= ENSP00000382718.2:n.-19T=
NM_000529.2:c.-19T= MANE Select NP_000520.1:n.-19T=
NM_001291911.1:c.-19T= NP_001278840.1:n.-19T=
XM_017025781.1:c.-19T= XP_016881270.1:n.-19T=