Canonical Allele Identifier: CA730295507
Gene:

Linked Data

dbSNP Id: rs1490463312
gnomAD v3: 1-2036470-C-T
gnomAD v4: 1-2036470-C-T
MyVariant Identifiers: chr1:g.1967909C>T (hg19) chr1:g.2036470C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2036470C>T , CM000663.2:g.2036470C>T GRCh38
NC_000001.10:g.1967909C>T , CM000663.1:g.1967909C>T GRCh37
NC_000001.9:g.1957769C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_946823.1:n.738G>A
XR_001737845.2:n.741G>A
XR_946823.3:n.741G>A
Search 100 bp 5'
Search 100 bp 3'