Canonical Allele Identifier: CA890857180
Gene:

Linked Data

dbSNP Id: rs1446891713
gnomAD v3: 1-168649243-G-C
gnomAD v4: 1-168649243-G-C
MyVariant Identifiers: chr1:g.168618481G>C (hg19) chr1:g.168649243G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168649243G>C , CM000663.2:g.168649243G>C GRCh38
NC_000001.10:g.168618481G>C , CM000663.1:g.168618481G>C GRCh37
NC_000001.9:g.166885105G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922259.1:n.201-7968C>G
XR_922259.2:n.332-7968C>G
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