Canonical Allele Identifier: CA290050502
Gene:
MyVariant.info:
GRCh38 chr17:g.35870979C>T
gnomAD v3:
17:35870979 C / T
gnomAD v4:
chr17-35870979-C-T
Joint Max Group AF 0.3177755 (EAS)
Genomes Max Group AF 0.3177755 (EAS)
dbSNP:
9909416
JSON-LD

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
Search 100 bp 5'
Search 100 bp 3'