Canonical Allele Identifier: CA2255116959
Gene: BLMH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30248908G= , CM000679.2:g.30248908G= GRCh38
NC_000017.10:g.28575926G= , CM000679.1:g.28575926G= GRCh37
NC_000017.9:g.25600052G= NCBI36
NG_011440.1:g.48149C=

Transcript Alleles

HGVS Amino-acid change
ENST00000261714.11:c.*109C= MANE Select ENSP00000261714.6:n.*109C=
ENST00000261714.10:c.*109C= ENSP00000261714.6:n.*109C=
ENST00000578090.5:c.*1151C= ENSP00000462353.1:n.*1151C=
ENST00000578795.1:n.1376C=
NM_000386.3:c.*109C= NP_000377.1:n.*109C=
XR_934653.1:n.701-879G=
XR_934655.1:n.701-3166G=
NM_000386.4:c.*109C= MANE Select NP_000377.1:n.*109C=