Canonical Allele Identifier: CA595199221
Gene:

Linked Data

dbSNP Id: rs57970638
gnomAD v2: 10-103510313-G-T
gnomAD v3: 10-101750556-G-T
gnomAD v4: 10-101750556-G-T
MyVariant Identifiers: chr10:g.103510313G>T (hg19) chr10:g.101750556G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.101750556G>T , CM000672.2:g.101750556G>T GRCh38
NC_000010.10:g.103510313G>T , CM000672.1:g.103510313G>T GRCh37
NC_000010.9:g.103500303G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_946255.1:n.217-6339C>A
XR_946255.2:n.217-6339C>A
Search 100 bp 5'
Search 100 bp 3'