Canonical Allele Identifier: CA2255116954
Gene: BLMH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30248903A= , CM000679.2:g.30248903A= GRCh38
NC_000017.10:g.28575921A= , CM000679.1:g.28575921A= GRCh37
NC_000017.9:g.25600047A= NCBI36
NG_011440.1:g.48154T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261714.11:c.*114T= MANE Select ENSP00000261714.6:n.*114T=
ENST00000261714.10:c.*114T= ENSP00000261714.6:n.*114T=
ENST00000578090.5:c.*1156T= ENSP00000462353.1:n.*1156T=
ENST00000578795.1:n.1381T=
NM_000386.3:c.*114T= NP_000377.1:n.*114T=
XR_934653.1:n.701-884A=
XR_934655.1:n.701-3171A=
NM_000386.4:c.*114T= MANE Select NP_000377.1:n.*114T=