Canonical Allele Identifier: CA9894342

Gene: NCOA3

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.47627680C>T , CM000682.2:g.47627680C>T	GRCh38
NC_000020.10:g.46256424C>T , CM000682.1:g.46256424C>T	GRCh37
NC_000020.9:g.45689831C>T	NCBI36
NG_016810.1:g.130824C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_181659.3:c.652C>T MANE Select	NP_858045.1:p.Arg218Cys
ENST00000371998.8:c.652C>T MANE Select	ENSP00000361066.3:p.Arg218Cys
NM_001174087.1:c.652C>T	NP_001167558.1:p.Arg218Cys
NM_001174087.2:c.652C>T	NP_001167558.1:p.Arg218Cys
NM_001174088.1:c.652C>T	NP_001167559.1:p.Arg218Cys
NM_001174088.2:c.652C>T	NP_001167559.1:p.Arg218Cys
NM_006534.3:c.652C>T	NP_006525.2:p.Arg218Cys
NM_006534.4:c.652C>T	NP_006525.2:p.Arg218Cys
NM_181659.2:c.652C>T	NP_858045.1:p.Arg218Cys
ENST00000371997.3:c.652C>T	ENSP00000361065.3:p.Arg218Cys
ENST00000371998.7:c.652C>T	ENSP00000361066.3:p.Arg218Cys
ENST00000372004.7:c.652C>T	ENSP00000361073.1:p.Arg218Cys
ENST00000497292.1:n.295C>T