Canonical Allele Identifier: CA171706445
Gene:

Linked Data

dbSNP Id: rs1001158693
MyVariant Identifiers: chr8:g.5907430C>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.5907430C>G , CM000670.2:g.5907430C>G GRCh38
NC_000008.10:g.5764952C>G , CM000670.1:g.5764952C>G GRCh37
NC_000008.9:g.5752360C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_941374.1:n.308-7699G>C
XR_941375.1:n.308-7699G>C
XR_941376.1:n.406-7699G>C
XR_941377.1:n.308-7699G>C
XR_941378.1:n.216-7699G>C
XR_001745765.1:n.308-7699G>C
XR_001745766.1:n.406-7699G>C
XR_001745767.1:n.216-7699G>C
XR_001745768.1:n.308-7699G>C
XR_941374.2:n.308-7699G>C
XR_941375.2:n.308-7699G>C