Canonical Allele Identifier: CA21367833
Gene:

Linked Data

dbSNP Id: rs11590421
gnomAD v2: 1-38994115-G-A
gnomAD v3: 1-38528443-G-A
gnomAD v4: 1-38528443-G-A
MyVariant Identifiers: chr1:g.38994115G>A (hg19) chr1:g.38994115_38994118delinsAGCT (hg19) chr1:g.38528443G>A (hg38) chr1:g.38528443_38528446delinsAGCT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.38528443G>A , CM000663.2:g.38528443G>A GRCh38
NC_000001.10:g.38994115G>A , CM000663.1:g.38994115G>A GRCh37
NC_000001.9:g.38766702G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_947211.1:n.331+66G>A
XR_947211.2:n.327+66G>A
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