Canonical Allele Identifier: CA2565457321
Gene: MC2R HGNC NCBI

Linked Data

gnomAD v4: 18-13885582-A-AT
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13885584dup , CM000680.2:g.13885584dup GRCh38
NC_000018.9:g.13885583dup , CM000680.1:g.13885583dup GRCh37
NC_000018.8:g.13875583dup NCBI36
NG_011819.1:g.34954dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000327606.4:c.-65dup MANE Select ENSP00000333821.2:n.-65dup
ENST00000327606.3:c.-65dup ENSP00000333821.2:n.-65dup
ENST00000399821.2:c.-65dup ENSP00000382718.2:n.-65dup
NM_000529.2:c.-65dup MANE Select NP_000520.1:n.-65dup
NM_001291911.1:c.-65dup NP_001278840.1:n.-65dup
XM_017025781.1:c.-65dup XP_016881270.1:n.-65dup
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