Canonical Allele Identifier: CA323577634
Gene:

Linked Data

dbSNP Id: rs976771813
gnomAD v3: 22-36130015-A-T
gnomAD v4: 22-36130015-A-T
MyVariant Identifiers: chr22:g.36526063A>T (hg19) chr22:g.36130015A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36130015A>T , CM000684.2:g.36130015A>T GRCh38
NC_000022.10:g.36526063A>T , CM000684.1:g.36526063A>T GRCh37
NC_000022.9:g.34856009A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_430441.2:n.1547+3147T>A
XR_938219.1:n.2921T>A
XR_938220.1:n.2921T>A
XR_938221.1:n.1471+3847T>A
XR_001755516.2:n.4783T>A
XR_001755517.2:n.3010T>A
XR_001755518.2:n.4783T>A
XR_001755519.2:n.4783T>A
XR_001755520.2:n.4783T>A
XR_001755521.2:n.4783T>A
XR_001755522.2:n.1637-2242T>A
XR_001755525.2:n.1637-661T>A
XR_001755526.2:n.1637-2242T>A
XR_430441.4:n.1636+3147T>A
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