Canonical Allele Identifier: CA401995902
Gene: MC2R HGNC NCBI

Linked Data

dbSNP Id: rs369691563

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13885387G>C , CM000680.2:g.13885387G>C GRCh38
NC_000018.9:g.13885386G>C , CM000680.1:g.13885386G>C GRCh37
NC_000018.8:g.13875386G>C NCBI36
NG_011819.1:g.35150C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000327606.4:c.132C>G MANE Select ENSP00000333821.2:p.Ile44Met
ENST00000327606.3:c.132C>G ENSP00000333821.2:p.Ile44Met
ENST00000399821.2:c.132C>G ENSP00000382718.2:p.Ile44Met
NM_000529.2:c.132C>G MANE Select NP_000520.1:p.Ile44Met
NM_001291911.1:c.132C>G NP_001278840.1:p.Ile44Met
XM_017025781.1:c.132C>G XP_016881270.1:p.Ile44Met