Canonical Allele Identifier: CA16841781
Gene:

Linked Data

dbSNP Id: rs376312618
MyVariant Identifiers: chr1:g.1968030T>G (hg19) chr1:g.2036591T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2036591T>G , CM000663.2:g.2036591T>G GRCh38
NC_000001.10:g.1968030T>G , CM000663.1:g.1968030T>G GRCh37
NC_000001.9:g.1957890T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_946823.1:n.617A>C
XR_001737845.2:n.620A>C
XR_946823.3:n.620A>C
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