Canonical Allele Identifier: CA171706452
Gene:

Linked Data

dbSNP Id: rs980770120

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.5907451A>G , CM000670.2:g.5907451A>G GRCh38
NC_000008.10:g.5764973A>G , CM000670.1:g.5764973A>G GRCh37
NC_000008.9:g.5752381A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_941374.1:n.308-7720T>C
XR_941375.1:n.308-7720T>C
XR_941376.1:n.406-7720T>C
XR_941377.1:n.308-7720T>C
XR_941378.1:n.216-7720T>C
XR_001745765.1:n.308-7720T>C
XR_001745766.1:n.406-7720T>C
XR_001745767.1:n.216-7720T>C
XR_001745768.1:n.308-7720T>C
XR_941374.2:n.308-7720T>C
XR_941375.2:n.308-7720T>C