Canonical Allele Identifier: CA2255116960
Gene: BLMH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30248909T= , CM000679.2:g.30248909T= GRCh38
NC_000017.10:g.28575927T= , CM000679.1:g.28575927T= GRCh37
NC_000017.9:g.25600053T= NCBI36
NG_011440.1:g.48148A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261714.11:c.*108A= MANE Select ENSP00000261714.6:n.*108A=
ENST00000261714.10:c.*108A= ENSP00000261714.6:n.*108A=
ENST00000578090.5:c.*1150A= ENSP00000462353.1:n.*1150A=
ENST00000578795.1:n.1375A=
NM_000386.3:c.*108A= NP_000377.1:n.*108A=
XR_934653.1:n.701-878T=
XR_934655.1:n.701-3165T=
NM_000386.4:c.*108A= MANE Select NP_000377.1:n.*108A=