Canonical Allele Identifier: CA2637004688
Gene: BLMH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30248874A>C , CM000679.2:g.30248874A>C GRCh38
NC_000017.10:g.28575892A>C , CM000679.1:g.28575892A>C GRCh37
NC_000017.9:g.25600018A>C NCBI36
NG_011440.1:g.48183T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261714.11:c.*143T>G MANE Select ENSP00000261714.6:n.*143T>G
ENST00000261714.10:c.*143T>G ENSP00000261714.6:n.*143T>G
ENST00000578090.5:c.*1185T>G ENSP00000462353.1:n.*1185T>G
ENST00000578795.1:n.1410T>G
NM_000386.3:c.*143T>G NP_000377.1:n.*143T>G
XR_934653.1:n.701-913A>C
XR_934655.1:n.701-3200A>C
NM_000386.4:c.*143T>G MANE Select NP_000377.1:n.*143T>G