Canonical Allele Identifier: CA310850165
Gene:

Linked Data

dbSNP Id: rs879840539
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.2470857_2470858delinsT , CM000682.2:g.2470857_2470858delinsT GRCh38
NC_000020.10:g.2451503_2451504delinsT , CM000682.1:g.2451503_2451504delinsT GRCh37
NC_000020.9:g.2399503_2399504delinsT NCBI36
NG_042057.1:g.4996_4997delinsA

Transcript Alleles

HGVS Amino-acid Change
ENST00000461548.1:c.305-3100_305-3099delinsA ENSP00000456213.1:n.305-3100_305-3099delinsA
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