Canonical Allele Identifier: CA409694915
Gene: MC3R HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.54824347C>G (hg19) chr20:g.56249291C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.56249291C>G , CM000682.2:g.56249291C>G GRCh38
NC_000020.10:g.54824347C>G , CM000682.1:g.54824347C>G GRCh37
NC_000020.9:g.54257754C>G NCBI36
NG_012200.1:g.5560C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000243911.2:c.448C>G MANE Select ENSP00000243911.2:p.Leu150Val
NM_019888.3:c.448C>G MANE Select NP_063941.3:p.Leu150Val
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Search 100 bp 3'