Canonical Allele Identifier: CA534638454
Gene:

Linked Data

dbSNP Id: rs1558824730
gnomAD v2: 2-88315869-G-A
gnomAD v3: 2-88016350-G-A
gnomAD v4: 2-88016350-G-A
MyVariant Identifiers: chr2:g.88315869_88315873delinsAGTTA (hg19) chr2:g.88016350_88016354delinsAGTTA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016350G>A , CM000664.2:g.88016350G>A GRCh38
NC_000002.11:g.88315869G>A , CM000664.1:g.88315869G>A GRCh37
NC_000002.10:g.88096984G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.695G>A
XR_940336.3:n.695G>A
Search 100 bp 5'
Search 100 bp 3'