Canonical Allele Identifier: CA486173102

Gene: SOS2

Linked Data

• gnomAD v4: 14-50130568-A-T
• MyVariant Identifiers: chr14:g.50597286A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50130568A>T , CM000676.2:g.50130568A>T	GRCh38
NC_000014.8:g.50597286A>T , CM000676.1:g.50597286A>T	GRCh37
NC_000014.7:g.49667036A>T	NCBI36
NG_051073.1:g.106126T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.3270T>A MANE Select	ENSP00000216373.5:p.Ser1090=
ENST00000216373.9:c.3270T>A	ENSP00000216373.5:p.Ser1090=
ENST00000543680.5:c.3171T>A	ENSP00000445328.1:p.Ser1057=
NM_006939.2:c.3270T>A	NP_008870.2:p.Ser1090=
XM_005268021.1:c.3090T>A	XP_005268078.1:p.Ser1030=
XM_011537103.1:c.3231T>A	XP_011535405.1:p.Ser1077=
NM_006939.3:c.3270T>A	NP_008870.2:p.Ser1090=
NM_006939.4:c.3270T>A MANE Select	NP_008870.2:p.Ser1090=