Canonical Allele Identifier: CA503248443
Gene: MC2R HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.13885149C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13885150C>G , CM000680.2:g.13885150C>G GRCh38
NC_000018.9:g.13885149C>G , CM000680.1:g.13885149C>G GRCh37
NC_000018.8:g.13875149C>G NCBI36
NG_011819.1:g.35387G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000327606.4:c.369G>C MANE Select ENSP00000333821.2:p.Val123=
ENST00000327606.3:c.369G>C ENSP00000333821.2:p.Val123=
ENST00000399821.2:c.369G>C ENSP00000382718.2:p.Val123=
NM_000529.2:c.369G>C MANE Select NP_000520.1:p.Val123=
NM_001291911.1:c.369G>C NP_001278840.1:p.Val123=
XM_017025781.1:c.369G>C XP_016881270.1:p.Val123=
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