Canonical Allele Identifier: CA31701840
Gene:

Linked Data

dbSNP Id: rs916906205
MyVariant Identifiers: chr1:g.168618712G>C (hg19) chr1:g.168649474G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168649474G>C , CM000663.2:g.168649474G>C GRCh38
NC_000001.10:g.168618712G>C , CM000663.1:g.168618712G>C GRCh37
NC_000001.9:g.166885336G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922259.1:n.201-8199C>G
XR_922259.2:n.332-8199C>G
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