Canonical Allele Identifier: CA760016756
Gene:

Linked Data

dbSNP Id: rs1329932388
MyVariant Identifiers: chr2:g.16639645_16639646insA (hg19) chr2:g.16458377_16458378insA (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.16458380dup , CM000664.2:g.16458380dup GRCh38
NC_000002.11:g.16639648dup , CM000664.1:g.16639648dup GRCh37
NC_000002.10:g.16503129dup NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939752.1:n.396-3284dup
Search 100 bp 5'
Search 100 bp 3'