Canonical Allele Identifier: CA2255116952
Gene: BLMH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30248890G= , CM000679.2:g.30248890G= GRCh38
NC_000017.10:g.28575908G= , CM000679.1:g.28575908G= GRCh37
NC_000017.9:g.25600034G= NCBI36
NG_011440.1:g.48167C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261714.11:c.*127C= MANE Select ENSP00000261714.6:n.*127C=
ENST00000261714.10:c.*127C= ENSP00000261714.6:n.*127C=
ENST00000578090.5:c.*1169C= ENSP00000462353.1:n.*1169C=
ENST00000578795.1:n.1394C=
NM_000386.3:c.*127C= NP_000377.1:n.*127C=
XR_934653.1:n.701-897G=
XR_934655.1:n.701-3184G=
NM_000386.4:c.*127C= MANE Select NP_000377.1:n.*127C=