Canonical Allele Identifier: CA2255116962
Gene: BLMH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30248913G= , CM000679.2:g.30248913G= GRCh38
NC_000017.10:g.28575931G= , CM000679.1:g.28575931G= GRCh37
NC_000017.9:g.25600057G= NCBI36
NG_011440.1:g.48144C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261714.11:c.*104C= MANE Select ENSP00000261714.6:n.*104C=
ENST00000261714.10:c.*104C= ENSP00000261714.6:n.*104C=
ENST00000578090.5:c.*1146C= ENSP00000462353.1:n.*1146C=
ENST00000578795.1:n.1371C=
NM_000386.3:c.*104C= NP_000377.1:n.*104C=
XR_934653.1:n.701-874G=
XR_934655.1:n.701-3161G=
NM_000386.4:c.*104C= MANE Select NP_000377.1:n.*104C=