Canonical Allele Identifier: CA1760507421
Gene:

Linked Data

dbSNP Id: rs570994368

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.5907031G>T , CM000670.2:g.5907031G>T GRCh38
NC_000008.10:g.5764553G>T , CM000670.1:g.5764553G>T GRCh37
NC_000008.9:g.5751961G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_941374.1:n.308-7300C>A
XR_941375.1:n.308-7300C>A
XR_941376.1:n.406-7300C>A
XR_941377.1:n.308-7300C>A
XR_941378.1:n.216-7300C>A
XR_001745765.1:n.308-7300C>A
XR_001745766.1:n.406-7300C>A
XR_001745767.1:n.216-7300C>A
XR_001745768.1:n.308-7300C>A
XR_941374.2:n.308-7300C>A
XR_941375.2:n.308-7300C>A