Canonical Allele Identifier: CA401118838

Gene: H3-3B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75779150G>A , CM000679.2:g.75779150G>A	GRCh38
NC_000017.10:g.73775231G>A , CM000679.1:g.73775231G>A	GRCh37
NC_000017.9:g.71286826G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_005324.5:c.25C>T MANE Select	NP_005315.1:p.Arg9Cys
ENST00000254810.8:c.25C>T MANE Select	ENSP00000254810.3:p.Arg9Cys
NM_005324.4:c.25C>T	NP_005315.1:p.Arg9Cys
ENST00000586270.5:c.25C>T	ENSP00000465403.1:p.Arg9Cys
ENST00000586518.1:n.623C>T
ENST00000586607.5:c.25C>T	ENSP00000466020.1:p.Arg9Cys
ENST00000587171.1:c.25C>T	ENSP00000468484.1:p.Arg9Cys
ENST00000587560.5:c.25C>T	ENSP00000468714.1:p.Arg9Cys
ENST00000589417.1:n.158C>T
ENST00000589599.5:c.25C>T	ENSP00000465813.1:p.Arg9Cys
ENST00000589949.1:n.145C>T
ENST00000591890.5:c.25C>T	ENSP00000466663.1:p.Arg9Cys
ENST00000592643.5:c.25C>T	ENSP00000467165.1:p.Arg9Cys
ENST00000593254.1:n.118-268C>T