Canonical Allele Identifier: CA2673912766
Gene:

Linked Data

gnomAD v4: 5-56899989-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56899989T>A , CM000667.2:g.56899989T>A GRCh38
NC_000005.9:g.56195816T>A , CM000667.1:g.56195816T>A GRCh37
NC_000005.8:g.56231573T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948346.1:n.83-1693A>T
XR_948347.1:n.76+8A>T
XR_948347.3:n.406+8A>T