Canonical Allele Identifier: CA2637004696
Gene: BLMH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30248881C>A , CM000679.2:g.30248881C>A GRCh38
NC_000017.10:g.28575899C>A , CM000679.1:g.28575899C>A GRCh37
NC_000017.9:g.25600025C>A NCBI36
NG_011440.1:g.48176G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261714.11:c.*136G>T MANE Select ENSP00000261714.6:n.*136G>T
ENST00000261714.10:c.*136G>T ENSP00000261714.6:n.*136G>T
ENST00000578090.5:c.*1178G>T ENSP00000462353.1:n.*1178G>T
ENST00000578795.1:n.1403G>T
NM_000386.3:c.*136G>T NP_000377.1:n.*136G>T
XR_934653.1:n.701-906C>A
XR_934655.1:n.701-3193C>A
NM_000386.4:c.*136G>T MANE Select NP_000377.1:n.*136G>T