Canonical Allele Identifier: CA2575520262
Gene: SOS2 HGNC NCBI

Linked Data

gnomAD v4: 14-50130495-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50130495A>C , CM000676.2:g.50130495A>C GRCh38
NC_000014.8:g.50597213A>C , CM000676.1:g.50597213A>C GRCh37
NC_000014.7:g.49666963A>C NCBI36
NG_051073.1:g.106199T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000216373.10:c.3337+6T>G MANE Select ENSP00000216373.5:n.3337+6T>G
ENST00000216373.9:c.3337+6T>G ENSP00000216373.5:n.3337+6T>G
ENST00000543680.5:c.3238+6T>G ENSP00000445328.1:n.3238+6T>G
NM_006939.2:c.3337+6T>G NP_008870.2:n.3337+6T>G
XM_005268021.1:c.3157+6T>G XP_005268078.1:n.3157+6T>G
XM_011537103.1:c.3298+6T>G XP_011535405.1:n.3298+6T>G
NM_006939.3:c.3337+6T>G NP_008870.2:n.3337+6T>G
NM_006939.4:c.3337+6T>G MANE Select NP_008870.2:n.3337+6T>G
Search 100 bp 5'
Search 100 bp 3'