Canonical Allele Identifier: CA2624771075
Gene: SOS2 HGNC NCBI

Linked Data

gnomAD v4: 14-50150253-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50150253A>G , CM000676.2:g.50150253A>G GRCh38
NC_000014.8:g.50616971A>G , CM000676.1:g.50616971A>G GRCh37
NC_000014.7:g.49686721A>G NCBI36
NG_051073.1:g.86441T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000216373.10:c.2162-23T>C MANE Select ENSP00000216373.5:n.2162-23T>C
ENST00000216373.9:c.2162-23T>C ENSP00000216373.5:n.2162-23T>C
ENST00000543680.5:c.2063-23T>C ENSP00000445328.1:n.2063-23T>C
NM_006939.2:c.2162-23T>C NP_008870.2:n.2162-23T>C
XM_005268021.1:c.1982-23T>C XP_005268078.1:n.1982-23T>C
XM_011537103.1:c.2123-23T>C XP_011535405.1:n.2123-23T>C
XM_011537104.1:c.2162-23T>C XP_011535406.1:n.2162-23T>C
NM_006939.3:c.2162-23T>C NP_008870.2:n.2162-23T>C
NM_006939.4:c.2162-23T>C MANE Select NP_008870.2:n.2162-23T>C
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