Canonical Allele Identifier: CA2285919429
Gene: MC2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13885116C= , CM000680.2:g.13885116C= GRCh38
NC_000018.9:g.13885115C= , CM000680.1:g.13885115C= GRCh37
NC_000018.8:g.13875115C= NCBI36
NG_011819.1:g.35421G=

Transcript Alleles

HGVS Amino-acid change
ENST00000327606.4:c.403G= MANE Select ENSP00000333821.2:p.Ala135=
ENST00000327606.3:c.403G= ENSP00000333821.2:p.Ala135=
NM_000529.2:c.403G= MANE Select NP_000520.1:p.Ala135=
NM_001291911.1:c.403G= NP_001278840.1:p.Ala135=
XM_017025781.1:c.403G= XP_016881270.1:p.Ala135=