Canonical Allele Identifier: CA160899027

Gene: HSPB1

Linked Data

• ClinVar Variation Id: 2884503
• ClinVar RCV Id: RCV003617756
• dbSNP Id: rs557327165
• gnomAD v3: 7-76302828-C-G
• gnomAD v4: 7-76302828-C-G
• MyVariant Identifiers: chr7:g.75932145C>G (hg19) ; chr7:g.76302828C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.76302828C>G , CM000669.2:g.76302828C>G	GRCh38
NC_000007.13:g.75932145C>G , CM000669.1:g.75932145C>G	GRCh37
NC_000007.12:g.75770081C>G	NCBI36
NG_008995.1:g.5271C>G , LRG_248:g.5271C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000248553.7:c.116C>G MANE Select	ENSP00000248553.6:p.Pro39Arg
ENST00000674547.1:c.116C>G	ENSP00000502461.1:p.Pro39Arg
ENST00000674560.1:n.156C>G
ENST00000674638.1:c.116C>G	ENSP00000502651.1:p.Pro39Arg
ENST00000674650.1:c.116C>G	ENSP00000501628.1:p.Pro39Arg
ENST00000674965.1:c.116C>G	ENSP00000501765.1:p.Pro39Arg
ENST00000675134.1:c.116C>G	ENSP00000501831.1:p.Pro39Arg
ENST00000675226.1:c.116C>G	ENSP00000502510.1:p.Pro39Arg
ENST00000675488.1:n.156C>G
ENST00000675538.1:c.116C>G	ENSP00000502495.1:p.Pro39Arg
ENST00000675624.1:n.156C>G
ENST00000675733.1:n.156C>G
ENST00000675906.1:c.116C>G	ENSP00000502714.1:p.Pro39Arg
ENST00000676231.1:c.116C>G	ENSP00000502249.1:p.Pro39Arg
ENST00000676398.1:n.156C>G
ENST00000248553.6:c.116C>G	ENSP00000248553.6:p.Pro39Arg
ENST00000447574.1:c.116C>G	ENSP00000414357.1:p.Pro39Arg
NM_001540.3:c.116C>G , LRG_248t1:c.116C>G	NP_001531.1:p.Pro39Arg
NM_001540.4:c.116C>G	NP_001531.1:p.Pro39Arg
NM_001540.5:c.116C>G MANE Select	NP_001531.1:p.Pro39Arg