Canonical Allele Identifier: CA2285919581
Gene: MC2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13885495A= , CM000680.2:g.13885495A= GRCh38
NC_000018.9:g.13885494A= , CM000680.1:g.13885494A= GRCh37
NC_000018.8:g.13875494A= NCBI36
NG_011819.1:g.35042T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327606.4:c.24T= MANE Select ENSP00000333821.2:p.Tyr8=
ENST00000327606.3:c.24T= ENSP00000333821.2:p.Tyr8=
ENST00000399821.2:c.24T= ENSP00000382718.2:p.Tyr8=
NM_000529.2:c.24T= MANE Select NP_000520.1:p.Tyr8=
NM_001291911.1:c.24T= NP_001278840.1:p.Tyr8=
XM_017025781.1:c.24T= XP_016881270.1:p.Tyr8=