Canonical Allele Identifier: CA41486668
Gene:

Linked Data

dbSNP Id: rs34955430
MyVariant Identifiers: chr2:g.632790_632791insTTG (hg19) chr2:g.632790_632791insTTG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.632791_632792insTGT , CM000664.2:g.632791_632792insTGT GRCh38
NC_000002.11:g.632791_632792insTGT , CM000664.1:g.632791_632792insTGT GRCh37
NC_000002.10:g.622791_622792insTGT NCBI36
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