Canonical Allele Identifier: CA963008527
Gene: SOS2 HGNC NCBI

Linked Data

dbSNP Id: rs1348254699
gnomAD v3: 14-50152666-A-C
gnomAD v4: 14-50152666-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50152666A>C , CM000676.2:g.50152666A>C GRCh38
NC_000014.8:g.50619384A>C , CM000676.1:g.50619384A>C GRCh37
NC_000014.7:g.49689134A>C NCBI36
NG_051073.1:g.84028T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000216373.10:c.2161+404T>G MANE Select ENSP00000216373.5:n.2161+404T>G
ENST00000216373.9:c.2161+404T>G ENSP00000216373.5:n.2161+404T>G
ENST00000543680.5:c.2062+404T>G ENSP00000445328.1:n.2062+404T>G
NM_006939.2:c.2161+404T>G NP_008870.2:n.2161+404T>G
XM_005268021.1:c.1981+404T>G XP_005268078.1:n.1981+404T>G
XM_011537103.1:c.2122+404T>G XP_011535405.1:n.2122+404T>G
XM_011537104.1:c.2161+404T>G XP_011535406.1:n.2161+404T>G
NM_006939.3:c.2161+404T>G NP_008870.2:n.2161+404T>G
NM_006939.4:c.2161+404T>G MANE Select NP_008870.2:n.2161+404T>G
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