Canonical Allele Identifier: CA401996042
Gene: MC2R HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.13885453G>C (hg19) chr18:g.13885454G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13885454G>C , CM000680.2:g.13885454G>C GRCh38
NC_000018.9:g.13885453G>C , CM000680.1:g.13885453G>C GRCh37
NC_000018.8:g.13875453G>C NCBI36
NG_011819.1:g.35083C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000327606.4:c.65C>G MANE Select ENSP00000333821.2:p.Pro22Arg
ENST00000327606.3:c.65C>G ENSP00000333821.2:p.Pro22Arg
ENST00000399821.2:c.65C>G ENSP00000382718.2:p.Pro22Arg
NM_000529.2:c.65C>G MANE Select NP_000520.1:p.Pro22Arg
NM_001291911.1:c.65C>G NP_001278840.1:p.Pro22Arg
XM_017025781.1:c.65C>G XP_016881270.1:p.Pro22Arg
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