Canonical Allele Identifier: CA2255117008
Gene: BLMH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30249004C= , CM000679.2:g.30249004C= GRCh38
NC_000017.10:g.28576022C= , CM000679.1:g.28576022C= GRCh37
NC_000017.9:g.25600148C= NCBI36
NG_011440.1:g.48053G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261714.11:c.*13G= MANE Select ENSP00000261714.6:n.*13G=
ENST00000261714.10:c.*13G= ENSP00000261714.6:n.*13G=
ENST00000578090.5:c.*1055G= ENSP00000462353.1:n.*1055G=
ENST00000578795.1:n.1280G=
NM_000386.3:c.*13G= NP_000377.1:n.*13G=
XR_934653.1:n.701-783C=
XR_934655.1:n.701-3070C=
NM_000386.4:c.*13G= MANE Select NP_000377.1:n.*13G=