Canonical Allele Identifier: CA890857186
Gene:

Linked Data

dbSNP Id: rs1308225167
gnomAD v3: 1-168649253-C-T
gnomAD v4: 1-168649253-C-T
MyVariant Identifiers: chr1:g.168618491C>T (hg19) chr1:g.168649253C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168649253C>T , CM000663.2:g.168649253C>T GRCh38
NC_000001.10:g.168618491C>T , CM000663.1:g.168618491C>T GRCh37
NC_000001.9:g.166885115C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922259.1:n.201-7978G>A
XR_922259.2:n.332-7978G>A
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