Canonical Allele Identifier: CA2285919235
Gene: MC2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13884716T= , CM000680.2:g.13884716T= GRCh38
NC_000018.9:g.13884715T= , CM000680.1:g.13884715T= GRCh37
NC_000018.8:g.13874715T= NCBI36
NG_011819.1:g.35821A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327606.4:c.803A= MANE Select ENSP00000333821.2:p.Asn268=
ENST00000327606.3:c.803A= ENSP00000333821.2:p.Asn268=
NM_000529.2:c.803A= MANE Select NP_000520.1:p.Asn268=
NM_001291911.1:c.803A= NP_001278840.1:p.Asn268=
XM_017025781.1:c.803A= XP_016881270.1:p.Asn268=