Canonical Allele Identifier: CA1760507692
Gene:

Linked Data

dbSNP Id: rs1798577154

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.5907352G>A , CM000670.2:g.5907352G>A GRCh38
NC_000008.10:g.5764874G>A , CM000670.1:g.5764874G>A GRCh37
NC_000008.9:g.5752282G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_941374.1:n.308-7621C>T
XR_941375.1:n.308-7621C>T
XR_941376.1:n.406-7621C>T
XR_941377.1:n.308-7621C>T
XR_941378.1:n.216-7621C>T
XR_001745765.1:n.308-7621C>T
XR_001745766.1:n.406-7621C>T
XR_001745767.1:n.216-7621C>T
XR_001745768.1:n.308-7621C>T
XR_941374.2:n.308-7621C>T
XR_941375.2:n.308-7621C>T