Canonical Allele Identifier: CA2624771076
Gene: SOS2 HGNC NCBI

Linked Data

gnomAD v4: 14-50150254-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50150254A>T , CM000676.2:g.50150254A>T GRCh38
NC_000014.8:g.50616972A>T , CM000676.1:g.50616972A>T GRCh37
NC_000014.7:g.49686722A>T NCBI36
NG_051073.1:g.86440T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000216373.10:c.2162-24T>A MANE Select ENSP00000216373.5:n.2162-24T>A
ENST00000216373.9:c.2162-24T>A ENSP00000216373.5:n.2162-24T>A
ENST00000543680.5:c.2063-24T>A ENSP00000445328.1:n.2063-24T>A
NM_006939.2:c.2162-24T>A NP_008870.2:n.2162-24T>A
XM_005268021.1:c.1982-24T>A XP_005268078.1:n.1982-24T>A
XM_011537103.1:c.2123-24T>A XP_011535405.1:n.2123-24T>A
XM_011537104.1:c.2162-24T>A XP_011535406.1:n.2162-24T>A
NM_006939.3:c.2162-24T>A NP_008870.2:n.2162-24T>A
NM_006939.4:c.2162-24T>A MANE Select NP_008870.2:n.2162-24T>A
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