Canonical Allele Identifier: CA2621253706
Gene: HSPB8 HGNC NCBI

Linked Data

gnomAD v4: 12-119186998-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.119186998G>A , CM000674.2:g.119186998G>A GRCh38
NC_000012.11:g.119624803G>A , CM000674.1:g.119624803G>A GRCh37
NC_000012.10:g.118109186G>A NCBI36
NG_007953.2:g.13209G>A , LRG_249:g.13209G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000281938.7:c.368-27G>A MANE Select ENSP00000281938.3:n.368-27G>A
ENST00000674542.1:c.368-6701G>A ENSP00000502352.1:n.368-6701G>A
ENST00000674715.1:n.541-27G>A
ENST00000675900.1:n.21+4962G>A
ENST00000676071.1:n.101-27G>A
ENST00000676244.1:n.74-27G>A
ENST00000281938.6:c.368-27G>A ENSP00000281938.2:n.368-27G>A
ENST00000541798.1:c.91-27G>A
ENST00000542496.1:n.199G>A
NM_014365.2:c.368-27G>A , LRG_249t1:c.368-27G>A NP_055180.1:n.368-27G>A
NM_014365.3:c.368-27G>A MANE Select NP_055180.1:n.368-27G>A
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