Canonical Allele Identifier: CA171706350
Gene:

Linked Data

dbSNP Id: rs988712217
MyVariant Identifiers: chr8:g.5764509T>C (hg19) chr8:g.5906987T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.5906987T>C , CM000670.2:g.5906987T>C GRCh38
NC_000008.10:g.5764509T>C , CM000670.1:g.5764509T>C GRCh37
NC_000008.9:g.5751917T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_941374.1:n.308-7256A>G
XR_941375.1:n.308-7256A>G
XR_941376.1:n.406-7256A>G
XR_941377.1:n.308-7256A>G
XR_941378.1:n.216-7256A>G
XR_001745765.1:n.308-7256A>G
XR_001745766.1:n.406-7256A>G
XR_001745767.1:n.216-7256A>G
XR_001745768.1:n.308-7256A>G
XR_941374.2:n.308-7256A>G
XR_941375.2:n.308-7256A>G
Search 100 bp 5'
Search 100 bp 3'