Canonical Allele Identifier: CA2285919085
Gene: MC2R HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13884465C= , CM000680.2:g.13884465C= GRCh38
NC_000018.9:g.13884464C= , CM000680.1:g.13884464C= GRCh37
NC_000018.8:g.13874464C= NCBI36
NG_011819.1:g.36072G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327606.4:c.*160G= MANE Select ENSP00000333821.2:n.*160G=
ENST00000327606.3:c.*160G= ENSP00000333821.2:n.*160G=
NM_000529.2:c.*160G= MANE Select NP_000520.1:n.*160G=
NM_001291911.1:c.*160G= NP_001278840.1:n.*160G=
XM_017025781.1:c.*160G= XP_016881270.1:n.*160G=
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