Canonical Allele Identifier: CA534638463
Gene:

Linked Data

dbSNP Id: rs1229927199
gnomAD v2: 2-88315951-CCCCGTT-C
gnomAD v3: 2-88016432-CCCCGTT-C
gnomAD v4: 2-88016432-CCCCGTT-C
MyVariant Identifiers: chr2:g.88315952_88315957del (hg19) chr2:g.88016433_88016438del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016435_88016440del , CM000664.2:g.88016435_88016440del GRCh38
NC_000002.11:g.88315954_88315959del , CM000664.1:g.88315954_88315959del GRCh37
NC_000002.10:g.88097069_88097074del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.780_785del
XR_940336.3:n.780_785del
Search 100 bp 5'
Search 100 bp 3'