Canonical Allele Identifier: CA503248369

Gene: MC2R

Linked Data

• MyVariant Identifiers: chr18:g.13884912G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.13884913G>C , CM000680.2:g.13884913G>C	GRCh38
NC_000018.9:g.13884912G>C , CM000680.1:g.13884912G>C	GRCh37
NC_000018.8:g.13874912G>C	NCBI36
NG_011819.1:g.35624C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327606.4:c.606C>G MANE Select	ENSP00000333821.2:p.Ser202=
ENST00000327606.3:c.606C>G	ENSP00000333821.2:p.Ser202=
NM_000529.2:c.606C>G MANE Select	NP_000520.1:p.Ser202=
NM_001291911.1:c.606C>G	NP_001278840.1:p.Ser202=
XM_017025781.1:c.606C>G	XP_016881270.1:p.Ser202=