Canonical Allele Identifier: CA401996152
Gene: MC2R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13885502T>C , CM000680.2:g.13885502T>C GRCh38
NC_000018.9:g.13885501T>C , CM000680.1:g.13885501T>C GRCh37
NC_000018.8:g.13875501T>C NCBI36
NG_011819.1:g.35035A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000327606.4:c.17A>G MANE Select ENSP00000333821.2:p.Asn6Ser
ENST00000327606.3:c.17A>G ENSP00000333821.2:p.Asn6Ser
ENST00000399821.2:c.17A>G ENSP00000382718.2:p.Asn6Ser
NM_000529.2:c.17A>G MANE Select NP_000520.1:p.Asn6Ser
NM_001291911.1:c.17A>G NP_001278840.1:p.Asn6Ser
XM_017025781.1:c.17A>G XP_016881270.1:p.Asn6Ser