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ClinGen Allele Registry
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Canonical Allele Identifier:
CA2307359339
Community Standard Title: NM_005912.3(MC4R):c.148G= (p.Val50=)
Gene: MC4R
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.60372202C= , CM000680.2:g.60372202C=
GRCh38
NC_000018.9:g.58039435C= , CM000680.1:g.58039435C=
GRCh37
NC_000018.8:g.56190415C=
NCBI36
NG_016441.1:g.5567G=
Transcript Alleles
HGVS
Amino-acid Change
NM_005912.3:c.148G=
MANE Select
NP_005903.2:p.Val50=
ENST00000299766.5:c.148G=
MANE Select
ENSP00000299766.3:p.Val50=
NM_005912.2:c.148G=
NP_005903.2:p.Val50=
ENST00000299766.4:c.148G=
ENSP00000299766.3:p.Val50=
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