Canonical Allele Identifier: CA2307358959
Gene: MC4R HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.60371445T= , CM000680.2:g.60371445T= GRCh38
NC_000018.9:g.58038678T= , CM000680.1:g.58038678T= GRCh37
NC_000018.8:g.56189658T= NCBI36
NG_016441.1:g.6324A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299766.5:c.905A= MANE Select ENSP00000299766.3:p.Tyr302=
ENST00000299766.4:c.905A= ENSP00000299766.3:p.Tyr302=
NM_005912.2:c.905A= NP_005903.2:p.Tyr302=
NM_005912.3:c.905A= MANE Select NP_005903.2:p.Tyr302=
Search 100 bp 5'
Search 100 bp 3'