Canonical Allele Identifier: CA2630381758

Gene: BLM

Linked Data

• gnomAD v4: 15-90790598-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90790598T>C , CM000677.2:g.90790598T>C	GRCh38
NC_000015.9:g.91333828T>C , CM000677.1:g.91333828T>C	GRCh37
NC_000015.8:g.89134832T>C	NCBI36
NG_007272.1:g.78227T>C , LRG_20:g.78227T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000355112.8:c.2824-51T>C MANE Select	ENSP00000347232.3:n.2824-51T>C
ENST00000560559.2:n.1346T>C
ENST00000648453.1:c.2824-51T>C	ENSP00000497646.1:n.2824-51T>C
ENST00000680772.1:c.2824-51T>C	ENSP00000506117.1:n.2824-51T>C
ENST00000681142.1:c.2824-51T>C	ENSP00000506682.1:n.2824-51T>C
ENST00000355112.7:c.2824-51T>C	ENSP00000347232.3:n.2824-51T>C
ENST00000559724.5:c.*1748-51T>C	ENSP00000453359.1:n.*1748-51T>C
ENST00000560136.5:n.850-51T>C
ENST00000560509.5:c.2824-51T>C	ENSP00000454158.1:n.2824-51T>C
ENST00000560559.1:n.310T>C
NM_000057.3:c.2824-51T>C	NP_000048.1:n.2824-51T>C
NM_001287246.1:c.2824-51T>C	NP_001274175.1:n.2824-51T>C
NM_001287247.1:c.2824-51T>C	NP_001274176.1:n.2824-51T>C
NM_001287248.1:c.1699-51T>C	NP_001274177.1:n.1699-51T>C
XM_006720632.2:c.862-51T>C	XP_006720695.1:n.862-51T>C
XM_011521881.1:c.1510-51T>C	XP_011520183.1:n.1510-51T>C
XM_011521881.2:c.1510-51T>C	XP_011520183.1:n.1510-51T>C
NM_000057.4:c.2824-51T>C MANE Select	NP_000048.1:n.2824-51T>C
NM_001287246.2:c.2824-51T>C	NP_001274175.1:n.2824-51T>C
NM_001287247.2:c.2824-51T>C	NP_001274176.1:n.2824-51T>C
NM_001287248.2:c.1699-51T>C	NP_001274177.1:n.1699-51T>C