Canonical Allele Identifier: CA486173050
Gene: SOS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.50597223G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50130505G>T , CM000676.2:g.50130505G>T GRCh38
NC_000014.8:g.50597223G>T , CM000676.1:g.50597223G>T GRCh37
NC_000014.7:g.49666973G>T NCBI36
NG_051073.1:g.106189C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000216373.10:c.3333C>A MANE Select ENSP00000216373.5:p.Ser1111=
ENST00000216373.9:c.3333C>A ENSP00000216373.5:p.Ser1111=
ENST00000543680.5:c.3234C>A ENSP00000445328.1:p.Ser1078=
NM_006939.2:c.3333C>A NP_008870.2:p.Ser1111=
XM_005268021.1:c.3153C>A XP_005268078.1:p.Ser1051=
XM_011537103.1:c.3294C>A XP_011535405.1:p.Ser1098=
NM_006939.3:c.3333C>A NP_008870.2:p.Ser1111=
NM_006939.4:c.3333C>A MANE Select NP_008870.2:p.Ser1111=
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