Canonical Allele Identifier: CA255087092
Gene:

Linked Data

dbSNP Id: rs11070098
gnomAD v2: 13-95505262-T-C
gnomAD v3: 13-94853008-T-C
gnomAD v4: 13-94853008-T-C
MyVariant Identifiers: chr13:g.95505262T>C (hg19) chr13:g.94853008T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.94853008T>C , CM000675.2:g.94853008T>C GRCh38
NC_000013.10:g.95505262T>C , CM000675.1:g.95505262T>C GRCh37
NC_000013.9:g.94303263T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110754.1:n.257-52456T>C
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Search 100 bp 3'