Canonical Allele Identifier: CA528893600
Gene:

Linked Data

dbSNP Id: rs1308605084
gnomAD v2: 1-213855605-C-T
gnomAD v3: 1-213682262-C-T
gnomAD v4: 1-213682262-C-T
MyVariant Identifiers: chr1:g.213855605C>T (hg19) chr1:g.213682262C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.213682262C>T , CM000663.2:g.213682262C>T GRCh38
NC_000001.10:g.213855605C>T , CM000663.1:g.213855605C>T GRCh37
NC_000001.9:g.211922228C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001738463.1:n.601-49155C>T
XR_001738464.1:n.426-49155C>T
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Search 100 bp 3'