Canonical Allele Identifier: CA2255116961
Gene: BLMH HGNC NCBI

Linked Data

dbSNP Id: rs1907598951

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30248909T>A , CM000679.2:g.30248909T>A GRCh38
NC_000017.10:g.28575927T>A , CM000679.1:g.28575927T>A GRCh37
NC_000017.9:g.25600053T>A NCBI36
NG_011440.1:g.48148A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261714.11:c.*108A>T MANE Select ENSP00000261714.6:n.*108A>T
ENST00000261714.10:c.*108A>T ENSP00000261714.6:n.*108A>T
ENST00000578090.5:c.*1150A>T ENSP00000462353.1:n.*1150A>T
ENST00000578795.1:n.1375A>T
NM_000386.3:c.*108A>T NP_000377.1:n.*108A>T
XR_934653.1:n.701-878T>A
XR_934655.1:n.701-3165T>A
NM_000386.4:c.*108A>T MANE Select NP_000377.1:n.*108A>T