Canonical Allele Identifier: CA7738972

Gene: BLM

Linked Data

• ClinVar Variation Id: 236812
• ClinVar RCV Id: RCV000228367 ; RCV001019350 ; RCV003237782
• dbSNP Id: rs771767745
• ExAC: 15:91341447 G / A
• gnomAD v2: 15-91341447-G-A
• gnomAD v3: 15-90798217-G-A
• gnomAD v4: 15-90798217-G-A
• MyVariant Identifiers: chr15:g.91341447G>A (hg19) ; chr15:g.90798217G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90798217G>A , CM000677.2:g.90798217G>A	GRCh38
NC_000015.9:g.91341447G>A , CM000677.1:g.91341447G>A	GRCh37
NC_000015.8:g.89142451G>A	NCBI36
NG_007272.1:g.85846G>A , LRG_20:g.85846G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355112.8:c.3238G>A MANE Select	ENSP00000347232.3:p.Asp1080Asn
ENST00000560559.2:n.1811G>A
ENST00000648453.1:c.3238G>A	ENSP00000497646.1:p.Asp1080Asn
ENST00000680772.1:c.3238G>A	ENSP00000506117.1:p.Asp1080Asn
ENST00000681142.1:c.3238G>A	ENSP00000506682.1:p.Asp1080Asn
ENST00000355112.7:c.3238G>A	ENSP00000347232.3:p.Asp1080Asn
ENST00000558825.5:n.585G>A
ENST00000559724.5:c.*2162G>A	ENSP00000453359.1:n.*2162G>A
ENST00000560136.5:n.1264G>A
ENST00000560509.5:c.3238G>A	ENSP00000454158.1:p.Asp1080Asn
NM_000057.3:c.3238G>A	NP_000048.1:p.Asp1080Asn
NM_001287246.1:c.3238G>A	NP_001274175.1:p.Asp1080Asn
NM_001287247.1:c.3238G>A	NP_001274176.1:p.Asp1080Asn
NM_001287248.1:c.2113G>A	NP_001274177.1:p.Asp705Asn
XM_006720632.2:c.1276G>A	XP_006720695.1:p.Asp426Asn
XM_011521881.1:c.1924G>A	XP_011520183.1:p.Asp642Asn
XM_011521881.2:c.1924G>A	XP_011520183.1:p.Asp642Asn
NM_000057.4:c.3238G>A MANE Select	NP_000048.1:p.Asp1080Asn
NM_001287246.2:c.3238G>A	NP_001274175.1:p.Asp1080Asn
NM_001287247.2:c.3238G>A	NP_001274176.1:p.Asp1080Asn
NM_001287248.2:c.2113G>A	NP_001274177.1:p.Asp705Asn