Canonical Allele Identifier: CA2285919079
Gene: MC2R HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13884451A= , CM000680.2:g.13884451A= GRCh38
NC_000018.9:g.13884450A= , CM000680.1:g.13884450A= GRCh37
NC_000018.8:g.13874450A= NCBI36
NG_011819.1:g.36086T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327606.4:c.*174T= MANE Select ENSP00000333821.2:n.*174T=
ENST00000327606.3:c.*174T= ENSP00000333821.2:n.*174T=
NM_000529.2:c.*174T= MANE Select NP_000520.1:n.*174T=
NM_001291911.1:c.*174T= NP_001278840.1:n.*174T=
XM_017025781.1:c.*174T= XP_016881270.1:n.*174T=
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