Canonical Allele Identifier: CA2285919615
Gene: MC2R HGNC NCBI

Linked Data

dbSNP Id: rs2045271264
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13885556A>C , CM000680.2:g.13885556A>C GRCh38
NC_000018.9:g.13885555A>C , CM000680.1:g.13885555A>C GRCh37
NC_000018.8:g.13875555A>C NCBI36
NG_011819.1:g.34981T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000327606.4:c.-38T>G MANE Select ENSP00000333821.2:n.-38T>G
ENST00000327606.3:c.-38T>G ENSP00000333821.2:n.-38T>G
ENST00000399821.2:c.-38T>G ENSP00000382718.2:n.-38T>G
NM_000529.2:c.-38T>G MANE Select NP_000520.1:n.-38T>G
NM_001291911.1:c.-38T>G NP_001278840.1:n.-38T>G
XM_017025781.1:c.-38T>G XP_016881270.1:n.-38T>G
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