Canonical Allele Identifier: CA207989737
Gene:

Linked Data

dbSNP Id: rs16911099
MyVariant Identifiers: chr10:g.57812923G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812923G>A , CM000672.2:g.57812923G>A GRCh38
NC_000010.10:g.59572683G>A , CM000672.1:g.59572683G>A GRCh37
NC_000010.9:g.59242689G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945979.1:n.68+34369C>T
XR_001747454.1:n.85+34369C>T