Canonical Allele Identifier: CA2136058785
Gene: SOS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50130488A= , CM000676.2:g.50130488A= GRCh38
NC_000014.8:g.50597206A= , CM000676.1:g.50597206A= GRCh37
NC_000014.7:g.49666956A= NCBI36
NG_051073.1:g.106206T=

Transcript Alleles

HGVS Amino-acid change
ENST00000216373.10:c.3337+13T= MANE Select ENSP00000216373.5:n.3337+13T=
ENST00000216373.9:c.3337+13T= ENSP00000216373.5:n.3337+13T=
ENST00000543680.5:c.3238+13T= ENSP00000445328.1:n.3238+13T=
NM_006939.2:c.3337+13T= NP_008870.2:n.3337+13T=
XM_005268021.1:c.3157+13T= XP_005268078.1:n.3157+13T=
XM_011537103.1:c.3298+13T= XP_011535405.1:n.3298+13T=
NM_006939.3:c.3337+13T= NP_008870.2:n.3337+13T=
NM_006939.4:c.3337+13T= MANE Select NP_008870.2:n.3337+13T=
Search 100 bp 5'
Search 100 bp 3'