Canonical Allele Identifier: CA2255116941
Gene: BLMH HGNC NCBI

Linked Data

dbSNP Id: rs1907597095
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30248866C>T , CM000679.2:g.30248866C>T GRCh38
NC_000017.10:g.28575884C>T , CM000679.1:g.28575884C>T GRCh37
NC_000017.9:g.25600010C>T NCBI36
NG_011440.1:g.48191G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261714.11:c.*151G>A MANE Select ENSP00000261714.6:n.*151G>A
ENST00000261714.10:c.*151G>A ENSP00000261714.6:n.*151G>A
ENST00000578090.5:c.*1193G>A ENSP00000462353.1:n.*1193G>A
ENST00000578795.1:n.1418G>A
NM_000386.3:c.*151G>A NP_000377.1:n.*151G>A
XR_934653.1:n.701-921C>T
XR_934655.1:n.701-3208C>T
NM_000386.4:c.*151G>A MANE Select NP_000377.1:n.*151G>A
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