Canonical Allele Identifier: CA14510900
Gene: MC2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13914914G>A , CM000680.2:g.13914914G>A GRCh38
NC_000018.9:g.13914913G>A , CM000680.1:g.13914913G>A GRCh37
NC_000018.8:g.13904913G>A NCBI36
NG_011819.1:g.5623C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000327606.4:c.-129+574C>T MANE Select ENSP00000333821.2:n.-129+574C>T
ENST00000327606.3:c.-129+574C>T ENSP00000333821.2:n.-129+574C>T
ENST00000399821.2:c.-129+716C>T ENSP00000382718.2:n.-129+716C>T
NM_000529.2:c.-129+574C>T MANE Select NP_000520.1:n.-129+574C>T
NM_001291911.1:c.-129+716C>T NP_001278840.1:n.-129+716C>T
XM_017025781.1:c.-661+574C>T XP_016881270.1:n.-661+574C>T