Canonical Allele Identifier: CA725798441
Gene:

Linked Data

dbSNP Id: rs1271065460
gnomAD v3: 16-9249481-T-TG
gnomAD v4: 16-9249481-T-TG
MyVariant Identifiers: chr16:g.9343338_9343339insG (hg19) chr16:g.9249481_9249482insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9249483dup , CM000678.2:g.9249483dup GRCh38
NC_000016.9:g.9343340dup , CM000678.1:g.9343340dup GRCh37
NC_000016.8:g.9250841dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933054.1:n.70+64750dup
Search 100 bp 5'
Search 100 bp 3'