Canonical Allele Identifier: CA2285919052
Gene: MC2R HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13884391A= , CM000680.2:g.13884391A= GRCh38
NC_000018.9:g.13884390A= , CM000680.1:g.13884390A= GRCh37
NC_000018.8:g.13874390A= NCBI36
NG_011819.1:g.36146T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327606.4:c.*234T= MANE Select ENSP00000333821.2:n.*234T=
ENST00000327606.3:c.*234T= ENSP00000333821.2:n.*234T=
NM_000529.2:c.*234T= MANE Select NP_000520.1:n.*234T=
NM_001291911.1:c.*234T= NP_001278840.1:n.*234T=
XM_017025781.1:c.*234T= XP_016881270.1:n.*234T=
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