Canonical Allele Identifier: CA2307358905
Gene: MC4R HGNC NCBI

Linked Data

dbSNP Id: rs1222986036
gnomAD v4: 18-60371344-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.60371344T>G , CM000680.2:g.60371344T>G GRCh38
NC_000018.9:g.58038577T>G , CM000680.1:g.58038577T>G GRCh37
NC_000018.8:g.56189557T>G NCBI36
NG_016441.1:g.6425A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000299766.5:c.*7A>C MANE Select ENSP00000299766.3:n.*7A>C
ENST00000299766.4:c.*7A>C ENSP00000299766.3:n.*7A>C
NM_005912.2:c.*7A>C NP_005903.2:n.*7A>C
NM_005912.3:c.*7A>C MANE Select NP_005903.2:n.*7A>C
Search 100 bp 5'
Search 100 bp 3'