Canonical Allele Identifier: CA492157749

Gene: BLM

Linked Data

• dbSNP Id: rs1393792078
• MyVariant Identifiers: chr15:g.91354478C>G (hg19) ; chr15:g.90811248C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90811248C>G , CM000677.2:g.90811248C>G	GRCh38
NC_000015.9:g.91354478C>G , CM000677.1:g.91354478C>G	GRCh37
NC_000015.8:g.89155482C>G	NCBI36
NG_007272.1:g.98877C>G , LRG_20:g.98877C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355112.8:c.3918C>G MANE Select	ENSP00000347232.3:p.Gly1306=
ENST00000560559.2:n.2491C>G
ENST00000648453.1:c.3918C>G	ENSP00000497646.1:p.Gly1306=
ENST00000680772.1:c.3918C>G	ENSP00000506117.1:p.Gly1306=
ENST00000681142.1:c.3918C>G	ENSP00000506682.1:p.Gly1306=
ENST00000355112.7:c.3918C>G	ENSP00000347232.3:p.Gly1306=
ENST00000558825.5:n.1265C>G
ENST00000559724.5:c.*2842C>G	ENSP00000453359.1:n.*2842C>G
ENST00000560136.5:n.1944C>G
ENST00000560509.5:c.3525C>G	ENSP00000454158.1:p.Gly1175=
ENST00000560821.1:n.338C>G
NM_000057.3:c.3918C>G	NP_000048.1:p.Gly1306=
NM_001287246.1:c.3918C>G	NP_001274175.1:p.Gly1306=
NM_001287247.1:c.3525C>G	NP_001274176.1:p.Gly1175=
NM_001287248.1:c.2793C>G	NP_001274177.1:p.Gly931=
XM_006720632.2:c.1956C>G	XP_006720695.1:p.Gly652=
XM_011521881.1:c.2604C>G	XP_011520183.1:p.Gly868=
XM_011521881.2:c.2604C>G	XP_011520183.1:p.Gly868=
NM_000057.4:c.3918C>G MANE Select	NP_000048.1:p.Gly1306=
NM_001287246.2:c.3918C>G	NP_001274175.1:p.Gly1306=
NM_001287247.2:c.3525C>G	NP_001274176.1:p.Gly1175=
NM_001287248.2:c.2793C>G	NP_001274177.1:p.Gly931=