Canonical Allele Identifier: CA2255116964
Gene: BLMH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30248920C= , CM000679.2:g.30248920C= GRCh38
NC_000017.10:g.28575938C= , CM000679.1:g.28575938C= GRCh37
NC_000017.9:g.25600064C= NCBI36
NG_011440.1:g.48137G=

Transcript Alleles

HGVS Amino-acid change
ENST00000261714.11:c.*97G= MANE Select ENSP00000261714.6:n.*97G=
ENST00000261714.10:c.*97G= ENSP00000261714.6:n.*97G=
ENST00000578090.5:c.*1139G= ENSP00000462353.1:n.*1139G=
ENST00000578795.1:n.1364G=
NM_000386.3:c.*97G= NP_000377.1:n.*97G=
XR_934653.1:n.701-867C=
XR_934655.1:n.701-3154C=
NM_000386.4:c.*97G= MANE Select NP_000377.1:n.*97G=