Canonical Allele Identifier: CA2612218606
Gene:

Linked Data

gnomAD v4: 11-6318897-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6318897C>T , CM000673.2:g.6318897C>T GRCh38
NC_000011.9:g.6340127C>T , CM000673.1:g.6340127C>T GRCh37
NC_000011.8:g.6296703C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930997.1:n.720+677C>T
Search 100 bp 5'
Search 100 bp 3'