Canonical Allele Identifier: CA486173061
Gene: SOS2 HGNC NCBI

Linked Data

gnomAD v4: 14-50130526-T-C
MyVariant Identifiers: chr14:g.50597244T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50130526T>C , CM000676.2:g.50130526T>C GRCh38
NC_000014.8:g.50597244T>C , CM000676.1:g.50597244T>C GRCh37
NC_000014.7:g.49666994T>C NCBI36
NG_051073.1:g.106168A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000216373.10:c.3312A>G MANE Select ENSP00000216373.5:p.Leu1104=
ENST00000216373.9:c.3312A>G ENSP00000216373.5:p.Leu1104=
ENST00000543680.5:c.3213A>G ENSP00000445328.1:p.Leu1071=
NM_006939.2:c.3312A>G NP_008870.2:p.Leu1104=
XM_005268021.1:c.3132A>G XP_005268078.1:p.Leu1044=
XM_011537103.1:c.3273A>G XP_011535405.1:p.Leu1091=
NM_006939.3:c.3312A>G NP_008870.2:p.Leu1104=
NM_006939.4:c.3312A>G MANE Select NP_008870.2:p.Leu1104=
Search 100 bp 5'
Search 100 bp 3'