Canonical Allele Identifier: CA54965499
Gene:

Linked Data

dbSNP Id: rs562514986
gnomAD v2: 2-123126731-AAC-A
gnomAD v3: 2-122369155-AAC-A
gnomAD v4: 2-122369155-AAC-A
MyVariant Identifiers: chr2:g.123126732_123126733del (hg19) chr2:g.122369156_122369157del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122369161_122369162del , CM000664.2:g.122369161_122369162del GRCh38
NC_000002.11:g.123126737_123126738del , CM000664.1:g.123126737_123126738del GRCh37
NC_000002.10:g.122843207_122843208del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923278.1:n.556-23802_556-23801del
XR_001739684.1:n.556-23802_556-23801del
Search 100 bp 5'
Search 100 bp 3'