Canonical Allele Identifier: CA315579823

Gene: NCOA3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.47579861G>T , CM000682.2:g.47579861G>T	GRCh38
NC_000020.10:g.46208605G>T , CM000682.1:g.46208605G>T	GRCh37
NC_000020.9:g.45642012G>T	NCBI36
NG_016810.1:g.83005G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371998.8:c.-98-3322G>T MANE Select	ENSP00000361066.3:n.-98-3322G>T
ENST00000371997.3:c.-98-3322G>T	ENSP00000361065.3:n.-98-3322G>T
ENST00000371998.7:c.-98-3322G>T	ENSP00000361066.3:n.-98-3322G>T
ENST00000372004.7:c.-98-3322G>T	ENSP00000361073.1:n.-98-3322G>T
NM_001174087.1:c.-98-3322G>T	NP_001167558.1:n.-98-3322G>T
NM_001174088.1:c.-98-3322G>T	NP_001167559.1:n.-98-3322G>T
NM_006534.3:c.-98-3322G>T	NP_006525.2:n.-98-3322G>T
NM_181659.2:c.-98-3322G>T	NP_858045.1:n.-98-3322G>T
NM_181659.3:c.-98-3322G>T MANE Select	NP_858045.1:n.-98-3322G>T
NM_001174087.2:c.-98-3322G>T	NP_001167558.1:n.-98-3322G>T
NM_001174088.2:c.-98-3322G>T	NP_001167559.1:n.-98-3322G>T
NM_006534.4:c.-98-3322G>T	NP_006525.2:n.-98-3322G>T