Canonical Allele Identifier: CA756174621
Gene:

Linked Data

dbSNP Id: rs1165253948
MyVariant Identifiers: chr2:g.123126787_123126788insATAGAT (hg19) chr2:g.122369211_122369212insATAGAT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122369213_122369218dup , CM000664.2:g.122369213_122369218dup GRCh38
NC_000002.11:g.123126789_123126794dup , CM000664.1:g.123126789_123126794dup GRCh37
NC_000002.10:g.122843259_122843264dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923278.1:n.556-23750_556-23745dup
XR_001739684.1:n.556-23750_556-23745dup
Search 100 bp 5'
Search 100 bp 3'