Canonical Allele Identifier: CA797158829
Gene:

Linked Data

dbSNP Id: rs386356978
MyVariant Identifiers: chr4:g.63424165_63424166insC (hg19) chr4:g.62558447_62558448insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558449dup , CM000666.2:g.62558449dup GRCh38
NC_000004.11:g.63424167dup , CM000666.1:g.63424167dup GRCh37
NC_000004.10:g.63106762dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5395dup
Search 100 bp 5'
Search 100 bp 3'