Canonical Allele Identifier: CA14368384

Gene: SGSM2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.2359409C>T , CM000679.2:g.2359409C>T	GRCh38
NC_000017.10:g.2262703C>T , CM000679.1:g.2262703C>T	GRCh37
NC_000017.9:g.2209453C>T	NCBI36
NG_051965.1:g.26896C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268989.8:c.134-2228C>T MANE Select	ENSP00000268989.3:n.134-2228C>T
ENST00000268989.7:c.134-2228C>T	ENSP00000268989.3:n.134-2228C>T
ENST00000426855.6:c.134-2228C>T	ENSP00000415107.2:n.134-2228C>T
ENST00000572875.1:c.58-2228C>T	ENSP00000459218.2:n.58-2228C>T
ENST00000573062.5:c.134-2228C>T	ENSP00000476800.1:n.134-2228C>T
ENST00000574563.5:c.134-2228C>T	ENSP00000459126.1:n.134-2228C>T
NM_001098509.1:c.134-2228C>T	NP_001091979.1:n.134-2228C>T
NM_014853.2:c.134-2228C>T	NP_055668.2:n.134-2228C>T
XM_011524101.1:c.272-2228C>T	XP_011522403.1:n.272-2228C>T
XM_011524102.1:c.272-2228C>T	XP_011522404.1:n.272-2228C>T
XM_011524103.1:c.272-2228C>T	XP_011522405.1:n.272-2228C>T
XM_011524104.1:c.224-2228C>T	XP_011522406.1:n.224-2228C>T
XM_011524105.1:c.272-2228C>T	XP_011522407.1:n.272-2228C>T
XM_011524106.1:c.134-2228C>T	XP_011522408.1:n.134-2228C>T
XM_011524107.1:c.272-2228C>T	XP_011522409.1:n.272-2228C>T
XM_011524108.1:c.134-2228C>T	XP_011522410.1:n.134-2228C>T
XM_011524109.1:c.272-2228C>T	XP_011522411.1:n.272-2228C>T
XM_011524110.1:c.272-2228C>T	XP_011522412.1:n.272-2228C>T
XR_934127.1:n.373-2228C>T
XR_934128.1:n.373-2228C>T
XR_934129.1:n.373-2228C>T
NM_001346700.1:c.134-2228C>T	NP_001333629.1:n.134-2228C>T
XM_011524101.3:c.272-2228C>T	XP_011522403.1:n.272-2228C>T
XM_011524102.3:c.272-2228C>T	XP_011522404.1:n.272-2228C>T
XM_011524103.3:c.272-2228C>T	XP_011522405.1:n.272-2228C>T
XM_011524104.2:c.224-2228C>T	XP_011522406.1:n.224-2228C>T
XM_011524105.3:c.272-2228C>T	XP_011522407.1:n.272-2228C>T
XM_011524107.3:c.272-2228C>T	XP_011522409.1:n.272-2228C>T
XM_011524109.3:c.272-2228C>T	XP_011522411.1:n.272-2228C>T
XM_011524110.3:c.272-2228C>T	XP_011522412.1:n.272-2228C>T
XM_017025474.2:c.272-2228C>T	XP_016880963.1:n.272-2228C>T
XM_017025475.2:c.272-2228C>T	XP_016880964.1:n.272-2228C>T
XR_002958096.1:n.1469-2228C>T
XR_934127.3:n.1469-2228C>T
XR_934129.3:n.1469-2228C>T
NM_014853.3:c.134-2228C>T MANE Select	NP_055668.2:n.134-2228C>T
NM_001098509.2:c.134-2228C>T	NP_001091979.1:n.134-2228C>T
NM_001346700.2:c.134-2228C>T	NP_001333629.1:n.134-2228C>T