Canonical Allele Identifier: CA401994750
Gene: MC2R HGNC NCBI

Linked Data

dbSNP Id: rs104894659
MyVariant Identifiers: chr18:g.13884917G>C (hg19) chr18:g.13884918G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13884918G>C , CM000680.2:g.13884918G>C GRCh38
NC_000018.9:g.13884917G>C , CM000680.1:g.13884917G>C GRCh37
NC_000018.8:g.13874917G>C NCBI36
NG_011819.1:g.35619C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000327606.4:c.601C>G MANE Select ENSP00000333821.2:p.Arg201Gly
ENST00000327606.3:c.601C>G ENSP00000333821.2:p.Arg201Gly
NM_000529.2:c.601C>G MANE Select NP_000520.1:p.Arg201Gly
NM_001291911.1:c.601C>G NP_001278840.1:p.Arg201Gly
XM_017025781.1:c.601C>G XP_016881270.1:p.Arg201Gly
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