Canonical Allele Identifier: CA315599097

Gene: NCOA3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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