Canonical Allele Identifier: CA529297689
Gene:

Linked Data

dbSNP Id: rs1178881904
gnomAD v2: 1-220664984-ATT-A
gnomAD v3: 1-220491642-ATT-A
gnomAD v4: 1-220491642-ATT-A
MyVariant Identifiers: chr1:g.220664985_220664986del (hg19) chr1:g.220491643_220491644del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220491643_220491644del , CM000663.2:g.220491643_220491644del GRCh38
NC_000001.10:g.220664985_220664986del , CM000663.1:g.220664985_220664986del GRCh37
NC_000001.9:g.218731608_218731609del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922615.1:n.256-591_256-590del
XR_001737822.1:n.557-591_557-590del
Search 100 bp 5'
Search 100 bp 3'