Canonical Allele Identifier: CA171706348
Gene:

Linked Data

dbSNP Id: rs771418193
gnomAD v3: 8-5906976-C-T
gnomAD v4: 8-5906976-C-T
MyVariant Identifiers: chr8:g.5764498C>T (hg19) chr8:g.5906976C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.5906976C>T , CM000670.2:g.5906976C>T GRCh38
NC_000008.10:g.5764498C>T , CM000670.1:g.5764498C>T GRCh37
NC_000008.9:g.5751906C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_941374.1:n.308-7245G>A
XR_941375.1:n.308-7245G>A
XR_941376.1:n.406-7245G>A
XR_941377.1:n.308-7245G>A
XR_941378.1:n.216-7245G>A
XR_001745765.1:n.308-7245G>A
XR_001745766.1:n.406-7245G>A
XR_001745767.1:n.216-7245G>A
XR_001745768.1:n.308-7245G>A
XR_941374.2:n.308-7245G>A
XR_941375.2:n.308-7245G>A
Search 100 bp 5'
Search 100 bp 3'