Canonical Allele Identifier: CA2255116945
Gene: BLMH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30248883T= , CM000679.2:g.30248883T= GRCh38
NC_000017.10:g.28575901T= , CM000679.1:g.28575901T= GRCh37
NC_000017.9:g.25600027T= NCBI36
NG_011440.1:g.48174A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261714.11:c.*134A= MANE Select ENSP00000261714.6:n.*134A=
ENST00000261714.10:c.*134A= ENSP00000261714.6:n.*134A=
ENST00000578090.5:c.*1176A= ENSP00000462353.1:n.*1176A=
ENST00000578795.1:n.1401A=
NM_000386.3:c.*134A= NP_000377.1:n.*134A=
XR_934653.1:n.701-904T=
XR_934655.1:n.701-3191T=
NM_000386.4:c.*134A= MANE Select NP_000377.1:n.*134A=