Canonical Allele Identifier: CA614274484
Gene: SOS2 HGNC NCBI

Linked Data

dbSNP Id: rs566609381
gnomAD v2: 14-50616961-C-G
gnomAD v3: 14-50150243-C-G
gnomAD v4: 14-50150243-C-G
MyVariant Identifiers: chr14:g.50616961C>G (hg19) chr14:g.50150243C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50150243C>G , CM000676.2:g.50150243C>G GRCh38
NC_000014.8:g.50616961C>G , CM000676.1:g.50616961C>G GRCh37
NC_000014.7:g.49686711C>G NCBI36
NG_051073.1:g.86451G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000216373.10:c.2162-13G>C MANE Select ENSP00000216373.5:n.2162-13G>C
ENST00000216373.9:c.2162-13G>C ENSP00000216373.5:n.2162-13G>C
ENST00000543680.5:c.2063-13G>C ENSP00000445328.1:n.2063-13G>C
NM_006939.2:c.2162-13G>C NP_008870.2:n.2162-13G>C
XM_005268021.1:c.1982-13G>C XP_005268078.1:n.1982-13G>C
XM_011537103.1:c.2123-13G>C XP_011535405.1:n.2123-13G>C
XM_011537104.1:c.2162-13G>C XP_011535406.1:n.2162-13G>C
NM_006939.3:c.2162-13G>C NP_008870.2:n.2162-13G>C
NM_006939.4:c.2162-13G>C MANE Select NP_008870.2:n.2162-13G>C
Search 100 bp 5'
Search 100 bp 3'