Canonical Allele Identifier: CA2285919273
Gene: MC2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13884798A= , CM000680.2:g.13884798A= GRCh38
NC_000018.9:g.13884797A= , CM000680.1:g.13884797A= GRCh37
NC_000018.8:g.13874797A= NCBI36
NG_011819.1:g.35739T=

Transcript Alleles

HGVS Amino-acid change
ENST00000327606.4:c.721T= MANE Select ENSP00000333821.2:p.Leu241=
ENST00000327606.3:c.721T= ENSP00000333821.2:p.Leu241=
NM_000529.2:c.721T= MANE Select NP_000520.1:p.Leu241=
NM_001291911.1:c.721T= NP_001278840.1:p.Leu241=
XM_017025781.1:c.721T= XP_016881270.1:p.Leu241=