Canonical Allele Identifier: CA31701786
Gene:

Linked Data

dbSNP Id: rs538320986
MyVariant Identifiers: chr1:g.168649366C>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168649366C>A , CM000663.2:g.168649366C>A GRCh38
NC_000001.10:g.168618604C>A , CM000663.1:g.168618604C>A GRCh37
NC_000001.9:g.166885228C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922259.1:n.201-8091G>T
XR_922259.2:n.332-8091G>T