Canonical Allele Identifier: CA593764911
Gene:

Linked Data

dbSNP Id: rs1222839644
gnomAD v2: 10-59572730-G-T
gnomAD v3: 10-57812970-G-T
gnomAD v4: 10-57812970-G-T
MyVariant Identifiers: chr10:g.59572730G>T (hg19) chr10:g.57812970G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812970G>T , CM000672.2:g.57812970G>T GRCh38
NC_000010.10:g.59572730G>T , CM000672.1:g.59572730G>T GRCh37
NC_000010.9:g.59242736G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945979.1:n.68+34322C>A
XR_001747454.1:n.85+34322C>A
Search 100 bp 5'
Search 100 bp 3'