Canonical Allele Identifier: CA2612218610
Gene:

Linked Data

gnomAD v4: 11-6318901-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6318901C>T , CM000673.2:g.6318901C>T GRCh38
NC_000011.9:g.6340131C>T , CM000673.1:g.6340131C>T GRCh37
NC_000011.8:g.6296707C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930997.1:n.720+681C>T