Canonical Allele Identifier: CA871054655

Gene: SH2D1A STAG2

Linked Data

• dbSNP Id: rs1452581386
• gnomAD v3: X-124346285-A-G
• gnomAD v4: X-124346285-A-G
• MyVariant Identifiers: chrX:g.123480135A>G (hg19) ; chrX:g.124346285A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.124346285A>G , CM000685.2:g.124346285A>G	GRCh38
NC_000023.10:g.123480135A>G , CM000685.1:g.123480135A>G	GRCh37
NC_000023.9:g.123307816A>G	NCBI36
NG_007464.1:g.4986A>G , LRG_106:g.4986A>G
NG_033796.2:g.390726A>G , LRG_782:g.390726A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698112.1:n.499-19476A>G (SH2D1A)
ENST00000698113.1:c.-358A>G (SH2D1A)	ENSP00000513571.1:n.-358A>G
ENST00000469481.1:n.454-65537A>G (STAG2)
ENST00000635645.1:n.499-19476A>G (SH2D1A)
NM_001114937.2:c.-358A>G (SH2D1A)	NP_001108409.1:n.-358A>G
NM_002351.4:c.-358A>G , LRG_106t1:c.-358A>G (SH2D1A)	NP_002342.1:n.-358A>G