Canonical Allele Identifier: CA486173205

Gene: SOS2

Linked Data

• MyVariant Identifiers: chr14:g.50666547G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50199829G>A , CM000676.2:g.50199829G>A	GRCh38
NC_000014.8:g.50666547G>A , CM000676.1:g.50666547G>A	GRCh37
NC_000014.7:g.49736297G>A	NCBI36
NG_051073.1:g.36865C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216373.10:c.372C>T MANE Select	ENSP00000216373.5:p.Tyr124=
ENST00000216373.9:c.372C>T	ENSP00000216373.5:p.Tyr124=
ENST00000543680.5:c.372C>T	ENSP00000445328.1:p.Tyr124=
ENST00000555666.1:n.551C>T
ENST00000556469.5:n.343C>T
NM_006939.2:c.372C>T	NP_008870.2:p.Tyr124=
XM_005268021.1:c.192C>T	XP_005268078.1:p.Tyr64=
XM_011537103.1:c.333C>T	XP_011535405.1:p.Tyr111=
XM_011537104.1:c.372C>T	XP_011535406.1:p.Tyr124=
XR_943842.1:n.1039+15957G>A
XR_943843.1:n.1039+15957G>A
NM_006939.3:c.372C>T	NP_008870.2:p.Tyr124=
NM_006939.4:c.372C>T MANE Select	NP_008870.2:p.Tyr124=