Canonical Allele Identifier: CA310790644

Gene: SIRPG

Linked Data

• dbSNP Id: rs566035421
• gnomAD v3: 20-1629475-G-A
• gnomAD v4: 20-1629475-G-A
• MyVariant Identifiers: chr20:g.1610121G>A (hg19) ; chr20:g.1629475G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1629475G>A , CM000682.2:g.1629475G>A	GRCh38
NC_000020.10:g.1610121G>A , CM000682.1:g.1610121G>A	GRCh37
NC_000020.9:g.1558121G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000303415.7:c.*164C>T MANE Select	ENSP00000305529.3:n.*164C>T
ENST00000344103.8:c.*164C>T	ENSP00000342759.4:n.*164C>T
ENST00000381580.5:c.*164C>T	ENSP00000370992.1:n.*164C>T
ENST00000381583.6:c.*164C>T	ENSP00000370995.2:n.*164C>T
ENST00000478145.6:n.389C>T
NM_001039508.1:c.*164C>T	NP_001034597.1:n.*164C>T
NM_018556.3:c.*164C>T	NP_061026.2:n.*164C>T
NM_080816.2:c.*164C>T	NP_543006.2:n.*164C>T
XM_005260749.2:c.*164C>T	XP_005260806.1:n.*164C>T
XM_011529286.1:c.*164C>T	XP_011527588.1:n.*164C>T
XM_005260749.4:c.*164C>T	XP_005260806.1:n.*164C>T
XM_011529286.2:c.*164C>T	XP_011527588.1:n.*164C>T
NM_018556.4:c.*164C>T MANE Select	NP_061026.2:n.*164C>T
NM_080816.3:c.*164C>T	NP_543006.2:n.*164C>T
NM_001039508.2:c.*164C>T	NP_001034597.1:n.*164C>T