Canonical Allele Identifier: CA389649566
Gene: SOS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50199750T>C , CM000676.2:g.50199750T>C GRCh38
NC_000014.8:g.50666468T>C , CM000676.1:g.50666468T>C GRCh37
NC_000014.7:g.49736218T>C NCBI36
NG_051073.1:g.36944A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000216373.10:c.451A>G MANE Select ENSP00000216373.5:p.Asn151Asp
ENST00000216373.9:c.451A>G ENSP00000216373.5:p.Asn151Asp
ENST00000543680.5:c.451A>G ENSP00000445328.1:p.Asn151Asp
ENST00000555666.1:n.630A>G
ENST00000556469.5:n.422A>G
NM_006939.2:c.451A>G NP_008870.2:p.Asn151Asp
XM_005268021.1:c.271A>G XP_005268078.1:p.Asn91Asp
XM_011537103.1:c.412A>G XP_011535405.1:p.Asn138Asp
XM_011537104.1:c.451A>G XP_011535406.1:p.Asn151Asp
XR_943842.1:n.1039+15878T>C
XR_943843.1:n.1039+15878T>C
NM_006939.3:c.451A>G NP_008870.2:p.Asn151Asp
NM_006939.4:c.451A>G MANE Select NP_008870.2:p.Asn151Asp