Canonical Allele Identifier: CA54965528
Gene:

Linked Data

dbSNP Id: rs897587178
gnomAD v3: 2-122369291-ATT-A
gnomAD v4: 2-122369291-ATT-A
MyVariant Identifiers: chr2:g.123126868_123126869del (hg19) chr2:g.122369292_122369293del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122369292_122369293del , CM000664.2:g.122369292_122369293del GRCh38
NC_000002.11:g.123126868_123126869del , CM000664.1:g.123126868_123126869del GRCh37
NC_000002.10:g.122843338_122843339del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923278.1:n.556-23671_556-23670del
XR_001739684.1:n.556-23671_556-23670del
Search 100 bp 5'
Search 100 bp 3'