Canonical Allele Identifier: CA952405456
Gene: HSPB8 HGNC NCBI

Linked Data

dbSNP Id: rs1861838967
gnomAD v3: 12-119187006-A-G
gnomAD v4: 12-119187006-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.119187006A>G , CM000674.2:g.119187006A>G GRCh38
NC_000012.11:g.119624811A>G , CM000674.1:g.119624811A>G GRCh37
NC_000012.10:g.118109194A>G NCBI36
NG_007953.2:g.13217A>G , LRG_249:g.13217A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000281938.7:c.368-19A>G MANE Select ENSP00000281938.3:n.368-19A>G
ENST00000674542.1:c.368-6693A>G ENSP00000502352.1:n.368-6693A>G
ENST00000674715.1:n.541-19A>G
ENST00000675900.1:n.21+4970A>G
ENST00000676071.1:n.101-19A>G
ENST00000676244.1:n.74-19A>G
ENST00000281938.6:c.368-19A>G ENSP00000281938.2:n.368-19A>G
ENST00000541798.1:c.91-19A>G
ENST00000542496.1:n.207A>G
NM_014365.2:c.368-19A>G , LRG_249t1:c.368-19A>G NP_055180.1:n.368-19A>G
NM_014365.3:c.368-19A>G MANE Select NP_055180.1:n.368-19A>G
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