Canonical Allele Identifier: CA2255117018
Gene: BLMH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30249016A= , CM000679.2:g.30249016A= GRCh38
NC_000017.10:g.28576034A= , CM000679.1:g.28576034A= GRCh37
NC_000017.9:g.25600160A= NCBI36
NG_011440.1:g.48041T=

Transcript Alleles

HGVS Amino-acid change
ENST00000261714.11:c.*1T= MANE Select ENSP00000261714.6:n.*1T=
ENST00000261714.10:c.*1T= ENSP00000261714.6:n.*1T=
ENST00000578090.5:c.*1043T= ENSP00000462353.1:n.*1043T=
ENST00000578795.1:n.1268T=
NM_000386.3:c.*1T= NP_000377.1:n.*1T=
XR_934653.1:n.701-771A=
XR_934655.1:n.701-3058A=
NM_000386.4:c.*1T= MANE Select NP_000377.1:n.*1T=