Canonical Allele Identifier: CA486173049
Gene: SOS2 HGNC NCBI

Linked Data

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

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

Transcript Alleles

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