Canonical Allele Identifier: CA2255116946
Gene: BLMH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30248884G= , CM000679.2:g.30248884G= GRCh38
NC_000017.10:g.28575902G= , CM000679.1:g.28575902G= GRCh37
NC_000017.9:g.25600028G= NCBI36
NG_011440.1:g.48173C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261714.11:c.*133C= MANE Select ENSP00000261714.6:n.*133C=
ENST00000261714.10:c.*133C= ENSP00000261714.6:n.*133C=
ENST00000578090.5:c.*1175C= ENSP00000462353.1:n.*1175C=
ENST00000578795.1:n.1400C=
NM_000386.3:c.*133C= NP_000377.1:n.*133C=
XR_934653.1:n.701-903G=
XR_934655.1:n.701-3190G=
NM_000386.4:c.*133C= MANE Select NP_000377.1:n.*133C=