Canonical Allele Identifier: CA503248590

Gene: MC2R

Linked Data

• MyVariant Identifiers: chr18:g.13885215T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.13885216T>A , CM000680.2:g.13885216T>A	GRCh38
NC_000018.9:g.13885215T>A , CM000680.1:g.13885215T>A	GRCh37
NC_000018.8:g.13875215T>A	NCBI36
NG_011819.1:g.35321A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327606.4:c.303A>T MANE Select	ENSP00000333821.2:p.Thr101=
ENST00000327606.3:c.303A>T	ENSP00000333821.2:p.Thr101=
ENST00000399821.2:c.303A>T	ENSP00000382718.2:p.Thr101=
NM_000529.2:c.303A>T MANE Select	NP_000520.1:p.Thr101=
NM_001291911.1:c.303A>T	NP_001278840.1:p.Thr101=
XM_017025781.1:c.303A>T	XP_016881270.1:p.Thr101=