Canonical Allele Identifier: CA16614541

Gene: BLM

Linked Data

• ClinVar Variation Id: 405319
• ClinVar RCV Id: RCV000470527
• dbSNP Id: rs587778110
• MyVariant Identifiers: chr15:g.91306226A>G (hg19) ; chr15:g.90762996A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90762996A>G , CM000677.2:g.90762996A>G	GRCh38
NC_000015.9:g.91306226A>G , CM000677.1:g.91306226A>G	GRCh37
NC_000015.8:g.89107230A>G	NCBI36
NG_007272.1:g.50625A>G , LRG_20:g.50625A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355112.8:c.1913A>G MANE Select	ENSP00000347232.3:p.Asn638Ser
ENST00000648453.1:c.1913A>G	ENSP00000497646.1:p.Asn638Ser
ENST00000680772.1:c.1913A>G	ENSP00000506117.1:p.Asn638Ser
ENST00000681142.1:c.1913A>G	ENSP00000506682.1:p.Asn638Ser
ENST00000355112.7:c.1913A>G	ENSP00000347232.3:p.Asn638Ser
ENST00000559426.5:n.90A>G
ENST00000559724.5:c.*837A>G	ENSP00000453359.1:n.*837A>G
ENST00000560136.5:n.58A>G
ENST00000560509.5:c.1913A>G	ENSP00000454158.1:p.Asn638Ser
NM_000057.3:c.1913A>G	NP_000048.1:p.Asn638Ser
NM_001287246.1:c.1913A>G	NP_001274175.1:p.Asn638Ser
NM_001287247.1:c.1913A>G	NP_001274176.1:p.Asn638Ser
NM_001287248.1:c.788A>G	NP_001274177.1:p.Asn263Ser
XM_006720632.2:c.-50A>G	XP_006720695.1:n.-50A>G
XM_011521881.1:c.599A>G	XP_011520183.1:p.Asn200Ser
XM_011521882.1:c.1913A>G	XP_011520184.1:p.Asn638Ser
XM_011521881.2:c.599A>G	XP_011520183.1:p.Asn200Ser
XM_011521882.3:c.1913A>G	XP_011520184.1:p.Asn638Ser
NM_000057.4:c.1913A>G MANE Select	NP_000048.1:p.Asn638Ser
NM_001287246.2:c.1913A>G	NP_001274175.1:p.Asn638Ser
NM_001287247.2:c.1913A>G	NP_001274176.1:p.Asn638Ser
NM_001287248.2:c.788A>G	NP_001274177.1:p.Asn263Ser