Canonical Allele Identifier: CA823915604
Gene: HSPA1L HGNC NCBI

Linked Data

dbSNP Id: rs1008438
gnomAD v3: 6-31815431-A-T
gnomAD v4: 6-31815431-A-T
MyVariant Identifiers: chr6:g.31783208A>T (hg19) chr6:g.31815431A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31815431A>T , CM000668.2:g.31815431A>T GRCh38
NC_000006.11:g.31783208A>T , CM000668.1:g.31783208A>T GRCh37
NC_000006.10:g.31891187A>T NCBI36
NG_011855.1:g.4628T>A

Transcript Alleles

HGVS Amino-acid change
XM_005249071.1:c.-14+19T>A XP_005249128.1:n.-14+19T>A
XM_005249073.2:c.-13-3446T>A XP_005249130.1:n.-13-3446T>A
XM_011514566.1:c.-13-3446T>A XP_011512868.1:n.-13-3446T>A
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