Canonical Allele Identifier: CA504305530
Gene: MC4R HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.58038962G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.60371729G>T , CM000680.2:g.60371729G>T GRCh38
NC_000018.9:g.58038962G>T , CM000680.1:g.58038962G>T GRCh37
NC_000018.8:g.56189942G>T NCBI36
NG_016441.1:g.6040C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000299766.5:c.621C>A MANE Select ENSP00000299766.3:p.Leu207=
ENST00000299766.4:c.621C>A ENSP00000299766.3:p.Leu207=
NM_005912.2:c.621C>A NP_005903.2:p.Leu207=
NM_005912.3:c.621C>A MANE Select NP_005903.2:p.Leu207=
Search 100 bp 5'
Search 100 bp 3'