Canonical Allele Identifier: CA296828863

Gene: MC2R

Linked Data

• dbSNP Id: rs533512020
• MyVariant Identifiers: chr18:g.13885196A>T (hg19) ; chr18:g.13885197A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.13885197A>T , CM000680.2:g.13885197A>T	GRCh38
NC_000018.9:g.13885196A>T , CM000680.1:g.13885196A>T	GRCh37
NC_000018.8:g.13875196A>T	NCBI36
NG_011819.1:g.35340T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327606.4:c.322T>A MANE Select	ENSP00000333821.2:p.Ser108Thr
ENST00000327606.3:c.322T>A	ENSP00000333821.2:p.Ser108Thr
ENST00000399821.2:c.322T>A	ENSP00000382718.2:p.Ser108Thr
NM_000529.2:c.322T>A MANE Select	NP_000520.1:p.Ser108Thr
NM_001291911.1:c.322T>A	NP_001278840.1:p.Ser108Thr
XM_017025781.1:c.322T>A	XP_016881270.1:p.Ser108Thr