Canonical Allele Identifier: CA2624769281
Gene: SOS2 HGNC NCBI

Linked Data

gnomAD v4: 14-50130497-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50130497T>G , CM000676.2:g.50130497T>G GRCh38
NC_000014.8:g.50597215T>G , CM000676.1:g.50597215T>G GRCh37
NC_000014.7:g.49666965T>G NCBI36
NG_051073.1:g.106197A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000216373.10:c.3337+4A>C MANE Select ENSP00000216373.5:n.3337+4A>C
ENST00000216373.9:c.3337+4A>C ENSP00000216373.5:n.3337+4A>C
ENST00000543680.5:c.3238+4A>C ENSP00000445328.1:n.3238+4A>C
NM_006939.2:c.3337+4A>C NP_008870.2:n.3337+4A>C
XM_005268021.1:c.3157+4A>C XP_005268078.1:n.3157+4A>C
XM_011537103.1:c.3298+4A>C XP_011535405.1:n.3298+4A>C
NM_006939.3:c.3337+4A>C NP_008870.2:n.3337+4A>C
NM_006939.4:c.3337+4A>C MANE Select NP_008870.2:n.3337+4A>C
Search 100 bp 5'
Search 100 bp 3'