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UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
CA8902395
Gene: MC2R
HGNC
NCBI
Linked Data
dbSNP Id:
rs765604274
ExAC:
18:13884692 A / C
gnomAD v2:
18-13884692-A-C
gnomAD v3:
18-13884693-A-C
gnomAD v4:
18-13884693-A-C
MyVariant Identifiers:
chr18:g.13884692A>C (hg19)
chr18:g.13884693A>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.13884693A>C , CM000680.2:g.13884693A>C
GRCh38
NC_000018.9:g.13884692A>C , CM000680.1:g.13884692A>C
GRCh37
NC_000018.8:g.13874692A>C
NCBI36
NG_011819.1:g.35844T>G
Transcript Alleles
HGVS
Amino-acid change
ENST00000327606.4:c.826T>G
MANE Select
ENSP00000333821.2:p.Tyr276Asp
ENST00000327606.3:c.826T>G
ENSP00000333821.2:p.Tyr276Asp
NM_000529.2:c.826T>G
MANE Select
NP_000520.1:p.Tyr276Asp
NM_001291911.1:c.826T>G
NP_001278840.1:p.Tyr276Asp
XM_017025781.1:c.826T>G
XP_016881270.1:p.Tyr276Asp
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