Canonical Allele Identifier: CA310791226

Gene: SIRPG

Linked Data

• dbSNP Id: rs984858770
• gnomAD v2: 20-1610959-A-G
• gnomAD v3: 20-1630313-A-G
• gnomAD v4: 20-1630313-A-G
• MyVariant Identifiers: chr20:g.1610959A>G (hg19) ; chr20:g.1630313A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630313A>G , CM000682.2:g.1630313A>G	GRCh38
NC_000020.10:g.1610959A>G , CM000682.1:g.1610959A>G	GRCh37
NC_000020.9:g.1558959A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216927.4:c.749-7T>C	ENSP00000216927.4:n.749-7T>C
ENST00000303415.7:c.1082-7T>C MANE Select	ENSP00000305529.3:n.1082-7T>C
ENST00000344103.8:c.431-7T>C	ENSP00000342759.4:n.431-7T>C
ENST00000381580.5:c.983-7T>C	ENSP00000370992.1:n.983-7T>C
ENST00000381583.6:c.749-7T>C	ENSP00000370995.2:n.749-7T>C
ENST00000478145.6:n.143-7T>C
ENST00000497407.2:n.231-7T>C
NM_001039508.1:c.749-7T>C	NP_001034597.1:n.749-7T>C
NM_018556.3:c.1082-7T>C	NP_061026.2:n.1082-7T>C
NM_080816.2:c.431-7T>C	NP_543006.2:n.431-7T>C
XM_005260749.2:c.764-7T>C	XP_005260806.1:n.764-7T>C
XM_011529286.1:c.983-7T>C	XP_011527588.1:n.983-7T>C
XM_005260749.4:c.764-7T>C	XP_005260806.1:n.764-7T>C
XM_011529286.2:c.983-7T>C	XP_011527588.1:n.983-7T>C
NM_018556.4:c.1082-7T>C MANE Select	NP_061026.2:n.1082-7T>C
NM_080816.3:c.431-7T>C	NP_543006.2:n.431-7T>C
NM_001039508.2:c.749-7T>C	NP_001034597.1:n.749-7T>C