Canonical Allele Identifier: CA503248593

Gene: MC2R

Linked Data

• MyVariant Identifiers: chr18:g.13885008A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.13885009A>G , CM000680.2:g.13885009A>G	GRCh38
NC_000018.9:g.13885008A>G , CM000680.1:g.13885008A>G	GRCh37
NC_000018.8:g.13875008A>G	NCBI36
NG_011819.1:g.35528T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327606.4:c.510T>C MANE Select	ENSP00000333821.2:p.His170=
ENST00000327606.3:c.510T>C	ENSP00000333821.2:p.His170=
NM_000529.2:c.510T>C MANE Select	NP_000520.1:p.His170=
NM_001291911.1:c.510T>C	NP_001278840.1:p.His170=
XM_017025781.1:c.510T>C	XP_016881270.1:p.His170=