Canonical Allele Identifier: CA821223488
Gene:

Linked Data

dbSNP Id: rs1301239031
MyVariant Identifiers: chr6:g.156133482_156133483del (hg19) chr6:g.155812348_155812349del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812348_155812349del , CM000668.2:g.155812348_155812349del GRCh38
NC_000006.11:g.156133482_156133483del , CM000668.1:g.156133482_156133483del GRCh37
NC_000006.10:g.156175174_156175175del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+18929_79+18930del
XR_943146.1:n.645-310_645-309del
XR_001744423.1:n.699-310_699-309del
XR_001744424.1:n.79+18929_79+18930del
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