Canonical Allele Identifier: CA492164230

Gene: BLM

Linked Data

• dbSNP Id: rs2151184655
• gnomAD v4: 15-90790789-C-T
• MyVariant Identifiers: chr15:g.91334019C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90790789C>T , CM000677.2:g.90790789C>T	GRCh38
NC_000015.9:g.91334019C>T , CM000677.1:g.91334019C>T	GRCh37
NC_000015.8:g.89135023C>T	NCBI36
NG_007272.1:g.78418C>T , LRG_20:g.78418C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355112.8:c.2964C>T MANE Select	ENSP00000347232.3:p.His988=
ENST00000560559.2:n.1537C>T
ENST00000648453.1:c.2964C>T	ENSP00000497646.1:p.His988=
ENST00000680772.1:c.2964C>T	ENSP00000506117.1:p.His988=
ENST00000681142.1:c.2964C>T	ENSP00000506682.1:p.His988=
ENST00000355112.7:c.2964C>T	ENSP00000347232.3:p.His988=
ENST00000559724.5:c.*1888C>T	ENSP00000453359.1:n.*1888C>T
ENST00000560136.5:n.990C>T
ENST00000560509.5:c.2964C>T	ENSP00000454158.1:p.His988=
ENST00000560559.1:n.501C>T
NM_000057.3:c.2964C>T	NP_000048.1:p.His988=
NM_001287246.1:c.2964C>T	NP_001274175.1:p.His988=
NM_001287247.1:c.2964C>T	NP_001274176.1:p.His988=
NM_001287248.1:c.1839C>T	NP_001274177.1:p.His613=
XM_006720632.2:c.1002C>T	XP_006720695.1:p.His334=
XM_011521881.1:c.1650C>T	XP_011520183.1:p.His550=
XM_011521881.2:c.1650C>T	XP_011520183.1:p.His550=
NM_000057.4:c.2964C>T MANE Select	NP_000048.1:p.His988=
NM_001287246.2:c.2964C>T	NP_001274175.1:p.His988=
NM_001287247.2:c.2964C>T	NP_001274176.1:p.His988=
NM_001287248.2:c.1839C>T	NP_001274177.1:p.His613=