Canonical Allele Identifier: CA2612218650
Gene:

Linked Data

gnomAD v4: 11-6318930-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6318930T>A , CM000673.2:g.6318930T>A GRCh38
NC_000011.9:g.6340160T>A , CM000673.1:g.6340160T>A GRCh37
NC_000011.8:g.6296736T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930997.1:n.720+710T>A