Canonical Allele Identifier: CA2136058789
Gene: SOS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50130492A= , CM000676.2:g.50130492A= GRCh38
NC_000014.8:g.50597210A= , CM000676.1:g.50597210A= GRCh37
NC_000014.7:g.49666960A= NCBI36
NG_051073.1:g.106202T=

Transcript Alleles

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