Canonical Allele Identifier: CA2255116940
Gene: BLMH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30248866C= , CM000679.2:g.30248866C= GRCh38
NC_000017.10:g.28575884C= , CM000679.1:g.28575884C= GRCh37
NC_000017.9:g.25600010C= NCBI36
NG_011440.1:g.48191G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261714.11:c.*151G= MANE Select ENSP00000261714.6:n.*151G=
ENST00000261714.10:c.*151G= ENSP00000261714.6:n.*151G=
ENST00000578090.5:c.*1193G= ENSP00000462353.1:n.*1193G=
ENST00000578795.1:n.1418G=
NM_000386.3:c.*151G= NP_000377.1:n.*151G=
XR_934653.1:n.701-921C=
XR_934655.1:n.701-3208C=
NM_000386.4:c.*151G= MANE Select NP_000377.1:n.*151G=