Canonical Allele Identifier: CA2255117012
Gene: BLMH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30249009G= , CM000679.2:g.30249009G= GRCh38
NC_000017.10:g.28576027G= , CM000679.1:g.28576027G= GRCh37
NC_000017.9:g.25600153G= NCBI36
NG_011440.1:g.48048C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261714.11:c.*8C= MANE Select ENSP00000261714.6:n.*8C=
ENST00000261714.10:c.*8C= ENSP00000261714.6:n.*8C=
ENST00000578090.5:c.*1050C= ENSP00000462353.1:n.*1050C=
ENST00000578795.1:n.1275C=
NM_000386.3:c.*8C= NP_000377.1:n.*8C=
XR_934653.1:n.701-778G=
XR_934655.1:n.701-3065G=
NM_000386.4:c.*8C= MANE Select NP_000377.1:n.*8C=