Canonical Allele Identifier: CA401995389
Gene: MC2R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13885149T>G , CM000680.2:g.13885149T>G GRCh38
NC_000018.9:g.13885148T>G , CM000680.1:g.13885148T>G GRCh37
NC_000018.8:g.13875148T>G NCBI36
NG_011819.1:g.35388A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000327606.4:c.370A>C MANE Select ENSP00000333821.2:p.Ile124Leu
ENST00000327606.3:c.370A>C ENSP00000333821.2:p.Ile124Leu
ENST00000399821.2:c.370A>C
NM_000529.2:c.370A>C MANE Select NP_000520.1:p.Ile124Leu
NM_001291911.1:c.370A>C NP_001278840.1:p.Ile124Leu
XM_017025781.1:c.370A>C XP_016881270.1:p.Ile124Leu