Canonical Allele Identifier: CA393846420
Gene: BLM HGNC NCBI

Linked Data

ClinVar Variation Id: 843255
ClinVar RCV Id: RCV001045833
dbSNP Id: rs1051102270

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90790746A>C , CM000677.2:g.90790746A>C GRCh38
NC_000015.9:g.91333976A>C , CM000677.1:g.91333976A>C GRCh37
NC_000015.8:g.89134980A>C NCBI36
NG_007272.1:g.78375A>C , LRG_20:g.78375A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000355112.8:c.2921A>C MANE Select ENSP00000347232.3:p.Tyr974Ser
ENST00000560559.2:n.1494A>C
ENST00000648453.1:c.2921A>C ENSP00000497646.1:p.Tyr974Ser
ENST00000680772.1:c.2921A>C ENSP00000506117.1:p.Tyr974Ser
ENST00000681142.1:c.2921A>C ENSP00000506682.1:p.Tyr974Ser
ENST00000355112.7:c.2921A>C ENSP00000347232.3:p.Tyr974Ser
ENST00000559724.5:c.*1845A>C ENSP00000453359.1:n.*1845A>C
ENST00000560136.5:n.947A>C
ENST00000560509.5:c.2921A>C ENSP00000454158.1:p.Tyr974Ser
ENST00000560559.1:n.458A>C
NM_000057.3:c.2921A>C NP_000048.1:p.Tyr974Ser
NM_001287246.1:c.2921A>C NP_001274175.1:p.Tyr974Ser
NM_001287247.1:c.2921A>C NP_001274176.1:p.Tyr974Ser
NM_001287248.1:c.1796A>C NP_001274177.1:p.Tyr599Ser
XM_006720632.2:c.959A>C XP_006720695.1:p.Tyr320Ser
XM_011521881.1:c.1607A>C XP_011520183.1:p.Tyr536Ser
XM_011521881.2:c.1607A>C XP_011520183.1:p.Tyr536Ser
NM_000057.4:c.2921A>C MANE Select NP_000048.1:p.Tyr974Ser
NM_001287246.2:c.2921A>C NP_001274175.1:p.Tyr974Ser
NM_001287247.2:c.2921A>C NP_001274176.1:p.Tyr974Ser
NM_001287248.2:c.1796A>C NP_001274177.1:p.Tyr599Ser