Canonical Allele Identifier: CA632202292
Gene:

Linked Data

dbSNP Id: rs1224187879
gnomAD v2: 19-29035586-CCCT-C
gnomAD v3: 19-28544679-CCCT-C
gnomAD v4: 19-28544679-CCCT-C
MyVariant Identifiers: chr19:g.29035587_29035589del (hg19) chr19:g.28544680_28544682del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.28544684_28544686del , CM000681.2:g.28544684_28544686del GRCh38
NC_000019.9:g.29035591_29035593del , CM000681.1:g.29035591_29035593del GRCh37
NC_000019.8:g.33727431_33727433del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110759.1:n.657-77902_657-77900del
XR_243979.1:n.110-51659_110-51657del
Search 100 bp 5'
Search 100 bp 3'