Canonical Allele Identifier: CA504305529
Gene: MC4R HGNC NCBI

Linked Data

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

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

Transcript Alleles

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