Canonical Allele Identifier: CA2307359182
Gene: MC4R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.60371883T= , CM000680.2:g.60371883T= GRCh38
NC_000018.9:g.58039116T= , CM000680.1:g.58039116T= GRCh37
NC_000018.8:g.56190096T= NCBI36
NG_016441.1:g.5886A=

Transcript Alleles

HGVS Amino-acid change
ENST00000299766.5:c.467A= MANE Select ENSP00000299766.3:p.Gln156=
ENST00000299766.4:c.467A= ENSP00000299766.3:p.Gln156=
NM_005912.2:c.467A= NP_005903.2:p.Gln156=
NM_005912.3:c.467A= MANE Select NP_005903.2:p.Gln156=