Canonical Allele Identifier: CA2255116956
Gene: BLMH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30248904C= , CM000679.2:g.30248904C= GRCh38
NC_000017.10:g.28575922C= , CM000679.1:g.28575922C= GRCh37
NC_000017.9:g.25600048C= NCBI36
NG_011440.1:g.48153G=

Transcript Alleles

HGVS Amino-acid change
ENST00000261714.11:c.*113G= MANE Select ENSP00000261714.6:n.*113G=
ENST00000261714.10:c.*113G= ENSP00000261714.6:n.*113G=
ENST00000578090.5:c.*1155G= ENSP00000462353.1:n.*1155G=
ENST00000578795.1:n.1380G=
NM_000386.3:c.*113G= NP_000377.1:n.*113G=
XR_934653.1:n.701-883C=
XR_934655.1:n.701-3170C=
NM_000386.4:c.*113G= MANE Select NP_000377.1:n.*113G=