Canonical Allele Identifier: CA634123407

Gene: SIRPG

Linked Data

• dbSNP Id: rs1305783550
• gnomAD v2: 20-1611247-A-C
• gnomAD v3: 20-1630601-A-C
• gnomAD v4: 20-1630601-A-C
• MyVariant Identifiers: chr20:g.1611247A>C (hg19) ; chr20:g.1630601A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630601A>C , CM000682.2:g.1630601A>C	GRCh38
NC_000020.10:g.1611247A>C , CM000682.1:g.1611247A>C	GRCh37
NC_000020.9:g.1559247A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216927.4:c.749-295T>G	ENSP00000216927.4:n.749-295T>G
ENST00000303415.7:c.1082-295T>G MANE Select	ENSP00000305529.3:n.1082-295T>G
ENST00000344103.8:c.431-295T>G	ENSP00000342759.4:n.431-295T>G
ENST00000381580.5:c.983-295T>G	ENSP00000370992.1:n.983-295T>G
ENST00000381583.6:c.749-295T>G	ENSP00000370995.2:n.749-295T>G
ENST00000478145.6:n.142+94T>G
ENST00000497407.2:n.43T>G
NM_001039508.1:c.749-295T>G	NP_001034597.1:n.749-295T>G
NM_018556.3:c.1082-295T>G	NP_061026.2:n.1082-295T>G
NM_080816.2:c.431-295T>G	NP_543006.2:n.431-295T>G
XM_005260749.2:c.764-295T>G	XP_005260806.1:n.764-295T>G
XM_011529286.1:c.983-295T>G	XP_011527588.1:n.983-295T>G
XM_005260749.4:c.764-295T>G	XP_005260806.1:n.764-295T>G
XM_011529286.2:c.983-295T>G	XP_011527588.1:n.983-295T>G
NM_018556.4:c.1082-295T>G MANE Select	NP_061026.2:n.1082-295T>G
NM_080816.3:c.431-295T>G	NP_543006.2:n.431-295T>G
NM_001039508.2:c.749-295T>G	NP_001034597.1:n.749-295T>G