Canonical Allele Identifier: CA207989696
Gene:

Linked Data

dbSNP Id: rs528209792
gnomAD v2: 10-59572351-C-A
gnomAD v3: 10-57812591-C-A
gnomAD v4: 10-57812591-C-A
MyVariant Identifiers: chr10:g.59572351C>A (hg19) chr10:g.57812591C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812591C>A , CM000672.2:g.57812591C>A GRCh38
NC_000010.10:g.59572351C>A , CM000672.1:g.59572351C>A GRCh37
NC_000010.9:g.59242357C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945979.1:n.68+34701G>T
XR_001747454.1:n.85+34701G>T
Search 100 bp 5'
Search 100 bp 3'