Canonical Allele Identifier: CA393851344

Gene: BLM

Linked Data

• ClinVar Variation Id: 1061952
• ClinVar RCV Id: RCV001371617 ; RCV002357267
• dbSNP Id: rs2151199942
• gnomAD v4: 15-90811358-A-G
• MyVariant Identifiers: chr15:g.91354588A>G (hg19) ; chr15:g.90811358A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90811358A>G , CM000677.2:g.90811358A>G	GRCh38
NC_000015.9:g.91354588A>G , CM000677.1:g.91354588A>G	GRCh37
NC_000015.8:g.89155592A>G	NCBI36
NG_007272.1:g.98987A>G , LRG_20:g.98987A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355112.8:c.4028A>G MANE Select	ENSP00000347232.3:p.Gln1343Arg
ENST00000560559.2:n.2601A>G
ENST00000648453.1:c.4028A>G	ENSP00000497646.1:p.Gln1343Arg
ENST00000680772.1:c.4028A>G	ENSP00000506117.1:p.Gln1343Arg
ENST00000681142.1:c.4028A>G	ENSP00000506682.1:p.Gln1343Arg
ENST00000355112.7:c.4028A>G	ENSP00000347232.3:p.Gln1343Arg
ENST00000558825.5:n.1375A>G
ENST00000559724.5:c.*2952A>G	ENSP00000453359.1:n.*2952A>G
ENST00000560509.5:c.3635A>G	ENSP00000454158.1:p.Gln1212Arg
ENST00000560821.1:n.448A>G
NM_000057.3:c.4028A>G	NP_000048.1:p.Gln1343Arg
NM_001287246.1:c.4028A>G	NP_001274175.1:p.Gln1343Arg
NM_001287247.1:c.3635A>G	NP_001274176.1:p.Gln1212Arg
NM_001287248.1:c.2903A>G	NP_001274177.1:p.Gln968Arg
XM_006720632.2:c.2066A>G	XP_006720695.1:p.Gln689Arg
XM_011521881.1:c.2714A>G	XP_011520183.1:p.Gln905Arg
XM_011521881.2:c.2714A>G	XP_011520183.1:p.Gln905Arg
NM_000057.4:c.4028A>G MANE Select	NP_000048.1:p.Gln1343Arg
NM_001287246.2:c.4028A>G	NP_001274175.1:p.Gln1343Arg
NM_001287247.2:c.3635A>G	NP_001274176.1:p.Gln1212Arg
NM_001287248.2:c.2903A>G	NP_001274177.1:p.Gln968Arg