Canonical Allele Identifier: CA404644398

Gene: SIN3B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.16870061G>C , CM000681.2:g.16870061G>C	GRCh38
NC_000019.9:g.16980872G>C , CM000681.1:g.16980872G>C	GRCh37
NC_000019.8:g.16841872G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248054.10:c.2408G>C MANE Select	ENSP00000248054.4:p.Arg803Pro
ENST00000248054.9:c.2408G>C	ENSP00000248054.4:p.Arg803Pro
ENST00000379803.5:c.2504G>C	ENSP00000369131.1:p.Arg835Pro
ENST00000595541.1:c.1178G>C	ENSP00000469740.1:p.Arg393Pro
ENST00000595900.1:n.180G>C
ENST00000602204.1:n.93G>C
NM_001297595.1:c.2408G>C	NP_001284524.1:p.Arg803Pro
NM_001297597.1:c.1178G>C	NP_001284526.1:p.Arg393Pro
NM_015260.3:c.2504G>C	NP_056075.1:p.Arg835Pro
XM_006722704.1:c.953G>C	XP_006722767.1:p.Arg318Pro
NM_001297595.2:c.2408G>C MANE Select	NP_001284524.1:p.Arg803Pro
NM_015260.4:c.2504G>C	NP_056075.1:p.Arg835Pro
NM_001297597.2:c.1178G>C	NP_001284526.1:p.Arg393Pro