Canonical Allele Identifier: CA401994328
Gene: MC2R HGNC NCBI

Linked Data

dbSNP Id: rs770298010
gnomAD v4: 18-13884821-G-C
MyVariant Identifiers: chr18:g.13884820G>C (hg19) chr18:g.13884821G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13884821G>C , CM000680.2:g.13884821G>C GRCh38
NC_000018.9:g.13884820G>C , CM000680.1:g.13884820G>C GRCh37
NC_000018.8:g.13874820G>C NCBI36
NG_011819.1:g.35716C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000327606.4:c.698C>G MANE Select ENSP00000333821.2:p.Ala233Gly
ENST00000327606.3:c.698C>G ENSP00000333821.2:p.Ala233Gly
NM_000529.2:c.698C>G MANE Select NP_000520.1:p.Ala233Gly
NM_001291911.1:c.698C>G NP_001278840.1:p.Ala233Gly
XM_017025781.1:c.698C>G XP_016881270.1:p.Ala233Gly
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