Canonical Allele Identifier: CA619860850

Gene: BLM

Linked Data

• dbSNP Id: rs1364276313
• gnomAD v2: 15-91346706-A-C
• gnomAD v4: 15-90803476-A-C
• MyVariant Identifiers: chr15:g.91346706A>C (hg19) ; chr15:g.90803476A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90803476A>C , CM000677.2:g.90803476A>C	GRCh38
NC_000015.9:g.91346706A>C , CM000677.1:g.91346706A>C	GRCh37
NC_000015.8:g.89147710A>C	NCBI36
NG_007272.1:g.91105A>C , LRG_20:g.91105A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000355112.8:c.3359-45A>C MANE Select	ENSP00000347232.3:n.3359-45A>C
ENST00000560559.2:n.1932-45A>C
ENST00000648453.1:c.3359-45A>C	ENSP00000497646.1:n.3359-45A>C
ENST00000680772.1:c.3359-45A>C	ENSP00000506117.1:n.3359-45A>C
ENST00000681142.1:c.3359-45A>C	ENSP00000506682.1:n.3359-45A>C
ENST00000355112.7:c.3359-45A>C	ENSP00000347232.3:n.3359-45A>C
ENST00000558825.5:n.706-45A>C
ENST00000559724.5:c.*2283-45A>C	ENSP00000453359.1:n.*2283-45A>C
ENST00000560136.5:n.1385-45A>C
ENST00000560509.5:c.3358+5139A>C	ENSP00000454158.1:n.3358+5139A>C
NM_000057.3:c.3359-45A>C	NP_000048.1:n.3359-45A>C
NM_001287246.1:c.3359-45A>C	NP_001274175.1:n.3359-45A>C
NM_001287247.1:c.3358+5139A>C	NP_001274176.1:n.3358+5139A>C
NM_001287248.1:c.2234-45A>C	NP_001274177.1:n.2234-45A>C
XM_006720632.2:c.1397-45A>C	XP_006720695.1:n.1397-45A>C
XM_011521881.1:c.2045-45A>C	XP_011520183.1:n.2045-45A>C
XM_011521881.2:c.2045-45A>C	XP_011520183.1:n.2045-45A>C
NM_000057.4:c.3359-45A>C MANE Select	NP_000048.1:n.3359-45A>C
NM_001287246.2:c.3359-45A>C	NP_001274175.1:n.3359-45A>C
NM_001287247.2:c.3358+5139A>C	NP_001274176.1:n.3358+5139A>C
NM_001287248.2:c.2234-45A>C	NP_001274177.1:n.2234-45A>C