Canonical Allele Identifier: CA13330752
Gene:

Linked Data

dbSNP Id: rs2462021
gnomAD v2: 10-30490704-C-T
gnomAD v3: 10-30201775-C-T
gnomAD v4: 10-30201775-C-T
MyVariant Identifiers: chr10:g.30490704C>T (hg19) chr10:g.30201775C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30201775C>T , CM000672.2:g.30201775C>T GRCh38
NC_000010.10:g.30490704C>T , CM000672.1:g.30490704C>T GRCh37
NC_000010.9:g.30530710C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930791.1:n.1193-1712C>T
XR_930791.2:n.1449-1712C>T
Search 100 bp 5'
Search 100 bp 3'