Canonical Allele Identifier: CA2630381763
Gene: BLM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90790614C>A , CM000677.2:g.90790614C>A GRCh38
NC_000015.9:g.91333844C>A , CM000677.1:g.91333844C>A GRCh37
NC_000015.8:g.89134848C>A NCBI36
NG_007272.1:g.78243C>A , LRG_20:g.78243C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000355112.8:c.2824-35C>A MANE Select ENSP00000347232.3:n.2824-35C>A
ENST00000560559.2:n.1362C>A
ENST00000648453.1:c.2824-35C>A ENSP00000497646.1:n.2824-35C>A
ENST00000680772.1:c.2824-35C>A ENSP00000506117.1:n.2824-35C>A
ENST00000681142.1:c.2824-35C>A ENSP00000506682.1:n.2824-35C>A
ENST00000355112.7:c.2824-35C>A ENSP00000347232.3:n.2824-35C>A
ENST00000559724.5:c.*1748-35C>A ENSP00000453359.1:n.*1748-35C>A
ENST00000560136.5:n.850-35C>A
ENST00000560509.5:c.2824-35C>A ENSP00000454158.1:n.2824-35C>A
ENST00000560559.1:n.326C>A
NM_000057.3:c.2824-35C>A NP_000048.1:n.2824-35C>A
NM_001287246.1:c.2824-35C>A NP_001274175.1:n.2824-35C>A
NM_001287247.1:c.2824-35C>A NP_001274176.1:n.2824-35C>A
NM_001287248.1:c.1699-35C>A NP_001274177.1:n.1699-35C>A
XM_006720632.2:c.862-35C>A XP_006720695.1:n.862-35C>A
XM_011521881.1:c.1510-35C>A XP_011520183.1:n.1510-35C>A
XM_011521881.2:c.1510-35C>A XP_011520183.1:n.1510-35C>A
NM_000057.4:c.2824-35C>A MANE Select NP_000048.1:n.2824-35C>A
NM_001287246.2:c.2824-35C>A NP_001274175.1:n.2824-35C>A
NM_001287247.2:c.2824-35C>A NP_001274176.1:n.2824-35C>A
NM_001287248.2:c.1699-35C>A NP_001274177.1:n.1699-35C>A