Canonical Allele Identifier: CA531234604
Gene:

Linked Data

gnomAD v2: 2-16639511-TCTCAGC-T
gnomAD v3: 2-16458243-TCTCAGC-T
gnomAD v4: 2-16458243-TCTCAGC-T
MyVariant Identifiers: chr2:g.16639512_16639517del (hg19) chr2:g.16458244_16458249del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.16458244_16458249del , CM000664.2:g.16458244_16458249del GRCh38
NC_000002.11:g.16639512_16639517del , CM000664.1:g.16639512_16639517del GRCh37
NC_000002.10:g.16502993_16502998del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939752.1:n.396-3155_396-3150del
Search 100 bp 5'
Search 100 bp 3'