Canonical Allele Identifier: CA666857984
Gene:

Linked Data

dbSNP Id: rs1219595174
MyVariant Identifiers: chr10:g.59572407G>A (hg19) chr10:g.57812647G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812647G>A , CM000672.2:g.57812647G>A GRCh38
NC_000010.10:g.59572407G>A , CM000672.1:g.59572407G>A GRCh37
NC_000010.9:g.59242413G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945979.1:n.68+34645C>T
XR_001747454.1:n.85+34645C>T
Search 100 bp 5'
Search 100 bp 3'