Canonical Allele Identifier: CA393840789

Gene: BLM

Linked Data

• MyVariant Identifiers: chr15:g.91292952A>C (hg19) ; chr15:g.90749722A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90749722A>C , CM000677.2:g.90749722A>C	GRCh38
NC_000015.9:g.91292952A>C , CM000677.1:g.91292952A>C	GRCh37
NC_000015.8:g.89093956A>C	NCBI36
NG_007272.1:g.37351A>C , LRG_20:g.37351A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000355112.8:c.454A>C MANE Select	ENSP00000347232.3:p.Asn152His
ENST00000648453.1:c.454A>C	ENSP00000497646.1:p.Asn152His
ENST00000680772.1:c.454A>C	ENSP00000506117.1:p.Asn152His
ENST00000681142.1:c.454A>C	ENSP00000506682.1:p.Asn152His
ENST00000355112.7:c.454A>C	ENSP00000347232.3:p.Asn152His
ENST00000559282.1:n.628A>C
ENST00000559724.5:c.454A>C	ENSP00000453359.1:p.Asn152His
ENST00000560509.5:c.454A>C	ENSP00000454158.1:p.Asn152His
NM_000057.3:c.454A>C	NP_000048.1:p.Asn152His
NM_001287246.1:c.454A>C	NP_001274175.1:p.Asn152His
NM_001287247.1:c.454A>C	NP_001274176.1:p.Asn152His
NM_001287248.1:c.-838A>C	NP_001274177.1:n.-838A>C
XM_011521882.1:c.454A>C	XP_011520184.1:p.Asn152His
XM_011521882.3:c.454A>C	XP_011520184.1:p.Asn152His
NM_000057.4:c.454A>C MANE Select	NP_000048.1:p.Asn152His
NM_001287246.2:c.454A>C	NP_001274175.1:p.Asn152His
NM_001287247.2:c.454A>C	NP_001274176.1:p.Asn152His
NM_001287248.2:c.-838A>C	NP_001274177.1:n.-838A>C