Canonical Allele Identifier: CA2673912770
Gene:

Linked Data

gnomAD v4: 5-56899990-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56899990T>C , CM000667.2:g.56899990T>C GRCh38
NC_000005.9:g.56195817T>C , CM000667.1:g.56195817T>C GRCh37
NC_000005.8:g.56231574T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948346.1:n.83-1694A>G
XR_948347.1:n.76+7A>G
XR_948347.3:n.406+7A>G