Canonical Allele Identifier: CA2285919111
Gene: MC2R HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13884508T= , CM000680.2:g.13884508T= GRCh38
NC_000018.9:g.13884507T= , CM000680.1:g.13884507T= GRCh37
NC_000018.8:g.13874507T= NCBI36
NG_011819.1:g.36029A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327606.4:c.*117A= MANE Select ENSP00000333821.2:n.*117A=
ENST00000327606.3:c.*117A= ENSP00000333821.2:n.*117A=
NM_000529.2:c.*117A= MANE Select NP_000520.1:n.*117A=
NM_001291911.1:c.*117A= NP_001278840.1:n.*117A=
XM_017025781.1:c.*117A= XP_016881270.1:n.*117A=
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