Canonical Allele Identifier: CA2285919130
Gene: MC2R HGNC NCBI

Linked Data

dbSNP Id: rs2045259621
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13884537A>G , CM000680.2:g.13884537A>G GRCh38
NC_000018.9:g.13884536A>G , CM000680.1:g.13884536A>G GRCh37
NC_000018.8:g.13874536A>G NCBI36
NG_011819.1:g.36000T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000327606.4:c.*88T>C MANE Select ENSP00000333821.2:n.*88T>C
ENST00000327606.3:c.*88T>C ENSP00000333821.2:n.*88T>C
NM_000529.2:c.*88T>C MANE Select NP_000520.1:n.*88T>C
NM_001291911.1:c.*88T>C NP_001278840.1:n.*88T>C
XM_017025781.1:c.*88T>C XP_016881270.1:n.*88T>C
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