Canonical Allele Identifier: CA503248591
Gene: MC2R HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.13885215T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13885216T>C , CM000680.2:g.13885216T>C GRCh38
NC_000018.9:g.13885215T>C , CM000680.1:g.13885215T>C GRCh37
NC_000018.8:g.13875215T>C NCBI36
NG_011819.1:g.35321A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000327606.4:c.303A>G MANE Select ENSP00000333821.2:p.Thr101=
ENST00000327606.3:c.303A>G ENSP00000333821.2:p.Thr101=
ENST00000399821.2:c.303A>G ENSP00000382718.2:p.Thr101=
NM_000529.2:c.303A>G MANE Select NP_000520.1:p.Thr101=
NM_001291911.1:c.303A>G NP_001278840.1:p.Thr101=
XM_017025781.1:c.303A>G XP_016881270.1:p.Thr101=
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