Canonical Allele Identifier: CA625432862
Gene: BLMH HGNC NCBI

Linked Data

dbSNP Id: rs1382333526
gnomAD v2: 17-28575934-G-T
gnomAD v3: 17-30248916-G-T
gnomAD v4: 17-30248916-G-T
MyVariant Identifiers: chr17:g.28575934G>T (hg19) chr17:g.30248916G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30248916G>T , CM000679.2:g.30248916G>T GRCh38
NC_000017.10:g.28575934G>T , CM000679.1:g.28575934G>T GRCh37
NC_000017.9:g.25600060G>T NCBI36
NG_011440.1:g.48141C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261714.11:c.*101C>A MANE Select ENSP00000261714.6:n.*101C>A
ENST00000261714.10:c.*101C>A ENSP00000261714.6:n.*101C>A
ENST00000578090.5:c.*1143C>A ENSP00000462353.1:n.*1143C>A
ENST00000578795.1:n.1368C>A
NM_000386.3:c.*101C>A NP_000377.1:n.*101C>A
XR_934653.1:n.701-871G>T
XR_934655.1:n.701-3158G>T
NM_000386.4:c.*101C>A MANE Select NP_000377.1:n.*101C>A
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