Canonical Allele Identifier: CA890857333
Gene:

Linked Data

dbSNP Id: rs1425748067
gnomAD v3: 1-168649527-T-C
gnomAD v4: 1-168649527-T-C
MyVariant Identifiers: chr1:g.168618765T>C (hg19) chr1:g.168649527T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168649527T>C , CM000663.2:g.168649527T>C GRCh38
NC_000001.10:g.168618765T>C , CM000663.1:g.168618765T>C GRCh37
NC_000001.9:g.166885389T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922259.1:n.201-8252A>G
XR_922259.2:n.332-8252A>G
Search 100 bp 5'
Search 100 bp 3'