Canonical Allele Identifier: CA249282

Gene: BLM

Linked Data

• ClinVar Variation Id: 127493
• ClinVar RCV Id: RCV000203080 ; RCV000462198 ; RCV000561733 ; RCV000656777
• dbSNP Id: rs200690226
• ExAC: 15:91292772 A / G
• gnomAD v2: 15-91292772-A-G
• gnomAD v3: 15-90749542-A-G
• gnomAD v4: 15-90749542-A-G
• MyVariant Identifiers: chr15:g.91292772A>G (hg19) ; chr15:g.90749542A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90749542A>G , CM000677.2:g.90749542A>G	GRCh38
NC_000015.9:g.91292772A>G , CM000677.1:g.91292772A>G	GRCh37
NC_000015.8:g.89093776A>G	NCBI36
NG_007272.1:g.37171A>G , LRG_20:g.37171A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355112.8:c.274A>G MANE Select	ENSP00000347232.3:p.Asn92Asp
ENST00000648453.1:c.274A>G	ENSP00000497646.1:p.Asn92Asp
ENST00000680772.1:c.274A>G	ENSP00000506117.1:p.Asn92Asp
ENST00000681142.1:c.274A>G	ENSP00000506682.1:p.Asn92Asp
ENST00000355112.7:c.274A>G	ENSP00000347232.3:p.Asn92Asp
ENST00000559282.1:n.448A>G
ENST00000559724.5:c.274A>G	ENSP00000453359.1:p.Asn92Asp
ENST00000560509.5:c.274A>G	ENSP00000454158.1:p.Asn92Asp
NM_000057.3:c.274A>G	NP_000048.1:p.Asn92Asp
NM_001287246.1:c.274A>G	NP_001274175.1:p.Asn92Asp
NM_001287247.1:c.274A>G	NP_001274176.1:p.Asn92Asp
NM_001287248.1:c.-1018A>G	NP_001274177.1:n.-1018A>G
XM_011521882.1:c.274A>G	XP_011520184.1:p.Asn92Asp
XM_011521882.3:c.274A>G	XP_011520184.1:p.Asn92Asp
NM_000057.4:c.274A>G MANE Select	NP_000048.1:p.Asn92Asp
NM_001287246.2:c.274A>G	NP_001274175.1:p.Asn92Asp
NM_001287247.2:c.274A>G	NP_001274176.1:p.Asn92Asp
NM_001287248.2:c.-1018A>G	NP_001274177.1:n.-1018A>G