Canonical Allele Identifier: CA740538627
Gene:

Linked Data

dbSNP Id: rs1434509968
MyVariant Identifiers: chr1:g.95029581del (hg19) chr1:g.94564025del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94564026del , CM000663.2:g.94564026del GRCh38
NC_000001.10:g.95029582del , CM000663.1:g.95029582del GRCh37
NC_000001.9:g.94802170del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001738161.1:n.461+413del
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