Canonical Allele Identifier: CA2367203909

Gene: NCOA3

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.47604780C>A , CM000682.2:g.47604780C>A	GRCh38
NC_000020.10:g.46233524C>A , CM000682.1:g.46233524C>A	GRCh37
NC_000020.9:g.45666931C>A	NCBI36
NG_016810.1:g.107924C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371998.8:c.-19-17449C>A MANE Select	ENSP00000361066.3:n.-19-17449C>A
ENST00000371997.3:c.-19-17449C>A	ENSP00000361065.3:n.-19-17449C>A
ENST00000371998.7:c.-19-17449C>A	ENSP00000361066.3:n.-19-17449C>A
ENST00000372004.7:c.-19-17449C>A	ENSP00000361073.1:n.-19-17449C>A
NM_001174087.1:c.-19-17449C>A	NP_001167558.1:n.-19-17449C>A
NM_001174088.1:c.-19-17449C>A	NP_001167559.1:n.-19-17449C>A
NM_006534.3:c.-19-17449C>A	NP_006525.2:n.-19-17449C>A
NM_181659.2:c.-19-17449C>A	NP_858045.1:n.-19-17449C>A
NM_181659.3:c.-19-17449C>A MANE Select	NP_858045.1:n.-19-17449C>A
NM_001174087.2:c.-19-17449C>A	NP_001167558.1:n.-19-17449C>A
NM_001174088.2:c.-19-17449C>A	NP_001167559.1:n.-19-17449C>A
NM_006534.4:c.-19-17449C>A	NP_006525.2:n.-19-17449C>A