Canonical Allele Identifier: CA54965529
Gene:

Linked Data

dbSNP Id: rs1027341548
gnomAD v3: 2-122369294-C-G
gnomAD v4: 2-122369294-C-G
MyVariant Identifiers: chr2:g.123126870C>G (hg19) chr2:g.122369294C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122369294C>G , CM000664.2:g.122369294C>G GRCh38
NC_000002.11:g.123126870C>G , CM000664.1:g.123126870C>G GRCh37
NC_000002.10:g.122843340C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923278.1:n.556-23669C>G
XR_001739684.1:n.556-23669C>G
Search 100 bp 5'
Search 100 bp 3'