Canonical Allele Identifier: CA401995754

Gene: MC2R

Linked Data

• MyVariant Identifiers: chr18:g.13885321A>G (hg19) ; chr18:g.13885322A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.13885322A>G , CM000680.2:g.13885322A>G	GRCh38
NC_000018.9:g.13885321A>G , CM000680.1:g.13885321A>G	GRCh37
NC_000018.8:g.13875321A>G	NCBI36
NG_011819.1:g.35215T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327606.4:c.197T>C MANE Select	ENSP00000333821.2:p.Leu66Ser
ENST00000327606.3:c.197T>C	ENSP00000333821.2:p.Leu66Ser
ENST00000399821.2:c.197T>C	ENSP00000382718.2:p.Leu66Ser
NM_000529.2:c.197T>C MANE Select	NP_000520.1:p.Leu66Ser
NM_001291911.1:c.197T>C	NP_001278840.1:p.Leu66Ser
XM_017025781.1:c.197T>C	XP_016881270.1:p.Leu66Ser