Canonical Allele Identifier: CA520642660
Gene:

Linked Data

dbSNP Id: rs1445129353
gnomAD v2: 1-1967910-A-G
gnomAD v3: 1-2036471-A-G
gnomAD v4: 1-2036471-A-G
MyVariant Identifiers: chr1:g.1967910A>G (hg19) chr1:g.2036471A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2036471A>G , CM000663.2:g.2036471A>G GRCh38
NC_000001.10:g.1967910A>G , CM000663.1:g.1967910A>G GRCh37
NC_000001.9:g.1957770A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_946823.1:n.737T>C
XR_001737845.2:n.740T>C
XR_946823.3:n.740T>C
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