Canonical Allele Identifier: CA274764690

Gene: BLM

Linked Data

• ClinVar Variation Id: 822309
• ClinVar RCV Id: RCV001017573 ; RCV002550831
• dbSNP Id: rs1041847799
• MyVariant Identifiers: chr15:g.91333993G>A (hg19) ; chr15:g.90790763G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90790763G>A , CM000677.2:g.90790763G>A	GRCh38
NC_000015.9:g.91333993G>A , CM000677.1:g.91333993G>A	GRCh37
NC_000015.8:g.89134997G>A	NCBI36
NG_007272.1:g.78392G>A , LRG_20:g.78392G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355112.8:c.2938G>A MANE Select	ENSP00000347232.3:p.Ala980Thr
ENST00000560559.2:n.1511G>A
ENST00000648453.1:c.2938G>A	ENSP00000497646.1:p.Ala980Thr
ENST00000680772.1:c.2938G>A	ENSP00000506117.1:p.Ala980Thr
ENST00000681142.1:c.2938G>A	ENSP00000506682.1:p.Ala980Thr
ENST00000355112.7:c.2938G>A	ENSP00000347232.3:p.Ala980Thr
ENST00000559724.5:c.*1862G>A	ENSP00000453359.1:n.*1862G>A
ENST00000560136.5:n.964G>A
ENST00000560509.5:c.2938G>A	ENSP00000454158.1:p.Ala980Thr
ENST00000560559.1:n.475G>A
NM_000057.3:c.2938G>A	NP_000048.1:p.Ala980Thr
NM_001287246.1:c.2938G>A	NP_001274175.1:p.Ala980Thr
NM_001287247.1:c.2938G>A	NP_001274176.1:p.Ala980Thr
NM_001287248.1:c.1813G>A	NP_001274177.1:p.Ala605Thr
XM_006720632.2:c.976G>A	XP_006720695.1:p.Ala326Thr
XM_011521881.1:c.1624G>A	XP_011520183.1:p.Ala542Thr
XM_011521881.2:c.1624G>A	XP_011520183.1:p.Ala542Thr
NM_000057.4:c.2938G>A MANE Select	NP_000048.1:p.Ala980Thr
NM_001287246.2:c.2938G>A	NP_001274175.1:p.Ala980Thr
NM_001287247.2:c.2938G>A	NP_001274176.1:p.Ala980Thr
NM_001287248.2:c.1813G>A	NP_001274177.1:p.Ala605Thr