Canonical Allele Identifier: CA2641150754
Gene: MC2R HGNC NCBI

Linked Data

gnomAD v4: 18-13884593-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13884593C>A , CM000680.2:g.13884593C>A GRCh38
NC_000018.9:g.13884592C>A , CM000680.1:g.13884592C>A GRCh37
NC_000018.8:g.13874592C>A NCBI36
NG_011819.1:g.35944G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000327606.4:c.*32G>T MANE Select ENSP00000333821.2:n.*32G>T
ENST00000327606.3:c.*32G>T ENSP00000333821.2:n.*32G>T
NM_000529.2:c.*32G>T MANE Select NP_000520.1:n.*32G>T
NM_001291911.1:c.*32G>T NP_001278840.1:n.*32G>T
XM_017025781.1:c.*32G>T XP_016881270.1:n.*32G>T
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