Canonical Allele Identifier: CA2285919479
Gene: MC2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13885225A= , CM000680.2:g.13885225A= GRCh38
NC_000018.9:g.13885224A= , CM000680.1:g.13885224A= GRCh37
NC_000018.8:g.13875224A= NCBI36
NG_011819.1:g.35312T=

Transcript Alleles

HGVS Amino-acid change
ENST00000327606.4:c.294T= MANE Select ENSP00000333821.2:p.Phe98=
ENST00000327606.3:c.294T= ENSP00000333821.2:p.Phe98=
ENST00000399821.2:c.294T= ENSP00000382718.2:p.Phe98=
NM_000529.2:c.294T= MANE Select NP_000520.1:p.Phe98=
NM_001291911.1:c.294T= NP_001278840.1:p.Phe98=
XM_017025781.1:c.294T= XP_016881270.1:p.Phe98=