Canonical Allele Identifier: CA2255117009
Gene: BLMH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30249006G= , CM000679.2:g.30249006G= GRCh38
NC_000017.10:g.28576024G= , CM000679.1:g.28576024G= GRCh37
NC_000017.9:g.25600150G= NCBI36
NG_011440.1:g.48051C=

Transcript Alleles

HGVS Amino-acid change
ENST00000261714.11:c.*11C= MANE Select ENSP00000261714.6:n.*11C=
ENST00000261714.10:c.*11C= ENSP00000261714.6:n.*11C=
ENST00000578090.5:c.*1053C= ENSP00000462353.1:n.*1053C=
ENST00000578795.1:n.1278C=
NM_000386.3:c.*11C= NP_000377.1:n.*11C=
XR_934653.1:n.701-781G=
XR_934655.1:n.701-3068G=
NM_000386.4:c.*11C= MANE Select NP_000377.1:n.*11C=