Canonical Allele Identifier: CA290050502
Gene:

Linked Data

dbSNP Id: rs9909416
MyVariant Identifiers: chr17:g.35870979C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35870979C>T , CM000679.2:g.35870979C>T GRCh38
NC_000017.9:g.31222096C>T NCBI36
NG_015990.1:g.14395G>A

Transcript Alleles

HGVS Amino-acid Change
XR_934696.1:n.196+1861C>T
XR_934697.1:n.199+1861C>T
XR_934696.2:n.90+1861C>T
XR_934697.2:n.90+1861C>T