Canonical Allele Identifier: CA41419523
Gene:

Linked Data

dbSNP Id: rs954926105
MyVariant Identifiers: chr2:g.1557937_1557938insA (hg19) chr2:g.1554165_1554166insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.1554166dup , CM000664.2:g.1554166dup GRCh38
NC_000002.11:g.1557938dup , CM000664.1:g.1557938dup GRCh37
NC_000002.10:g.1536945dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510447.1:c.-1007dup XP_011508749.1:n.-1007dup
XM_011510448.1:c.-1007dup XP_011508750.1:n.-1007dup
XR_922720.1:n.85+2332dup
XM_017005455.1:c.-1007dup XP_016860944.1:n.-1007dup
NR_168373.1:n.746-4dup
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