Canonical Allele Identifier: CA535782183
Gene:

Linked Data

dbSNP Id: rs1302806091
gnomAD v2: 2-123126763-G-GCTAGATC
gnomAD v3: 2-122369187-G-GCTAGATC
gnomAD v4: 2-122369187-G-GCTAGATC
MyVariant Identifiers: chr2:g.123126763_123126764insCTAGATC (hg19) chr2:g.122369187_122369188insCTAGATC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122369193_122369194insCCTAGAT , CM000664.2:g.122369193_122369194insCCTAGAT GRCh38
NC_000002.11:g.123126769_123126770insCCTAGAT , CM000664.1:g.123126769_123126770insCCTAGAT GRCh37
NC_000002.10:g.122843239_122843240insCCTAGAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923278.1:n.556-23770_556-23769insCCTAGAT
XR_001739684.1:n.556-23770_556-23769insCCTAGAT
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