Canonical Allele Identifier: CA842327291

Gene: HSPB1

Linked Data

• dbSNP Id: rs1425827004
• gnomAD v4: 7-76303705-T-C
• MyVariant Identifiers: chr7:g.75933022T>C (hg19) ; chr7:g.76303705T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.76303705T>C , CM000669.2:g.76303705T>C	GRCh38
NC_000007.13:g.75933022T>C , CM000669.1:g.75933022T>C	GRCh37
NC_000007.12:g.75770958T>C	NCBI36
NG_008995.1:g.6148T>C , LRG_248:g.6148T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248553.7:c.365-97T>C MANE Select	ENSP00000248553.6:n.365-97T>C
ENST00000674547.1:c.365-97T>C	ENSP00000502461.1:n.365-97T>C
ENST00000674638.1:c.365-102T>C	ENSP00000502651.1:n.365-102T>C
ENST00000674650.1:c.365-279T>C	ENSP00000501628.1:n.365-279T>C
ENST00000674965.1:c.365-72T>C	ENSP00000501765.1:n.365-72T>C
ENST00000675134.1:c.365-97T>C	ENSP00000501831.1:n.365-97T>C
ENST00000675226.1:c.369-102T>C	ENSP00000502510.1:n.369-102T>C
ENST00000675417.1:n.501T>C
ENST00000675538.1:c.400-97T>C	ENSP00000502495.1:n.400-97T>C
ENST00000675733.1:n.405-57T>C
ENST00000675906.1:c.365-97T>C	ENSP00000502714.1:n.365-97T>C
ENST00000676195.1:n.80+49T>C
ENST00000676231.1:c.372T>C	ENSP00000502249.1:p.Ser124=
ENST00000248553.6:c.365-97T>C	ENSP00000248553.6:n.365-97T>C
ENST00000429938.1:c.-163T>C	ENSP00000405285.1:n.-163T>C
ENST00000447574.1:c.*432T>C	ENSP00000414357.1:n.*432T>C
NM_001540.3:c.365-97T>C , LRG_248t1:c.365-97T>C	NP_001531.1:n.365-97T>C
NM_001540.4:c.365-97T>C	NP_001531.1:n.365-97T>C
NM_001540.5:c.365-97T>C MANE Select	NP_001531.1:n.365-97T>C