Canonical Allele Identifier: CA2255116943
Gene: BLMH HGNC NCBI

Linked Data

dbSNP Id: rs1907597191

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30248869T>G , CM000679.2:g.30248869T>G GRCh38
NC_000017.10:g.28575887T>G , CM000679.1:g.28575887T>G GRCh37
NC_000017.9:g.25600013T>G NCBI36
NG_011440.1:g.48188A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261714.11:c.*148A>C MANE Select ENSP00000261714.6:n.*148A>C
ENST00000261714.10:c.*148A>C ENSP00000261714.6:n.*148A>C
ENST00000578090.5:c.*1190A>C ENSP00000462353.1:n.*1190A>C
ENST00000578795.1:n.1415A>C
NM_000386.3:c.*148A>C NP_000377.1:n.*148A>C
XR_934653.1:n.701-918T>G
XR_934655.1:n.701-3205T>G
NM_000386.4:c.*148A>C MANE Select NP_000377.1:n.*148A>C