Canonical Allele Identifier: CA2651630766
Gene:

Linked Data

gnomAD v4: 20-2470980-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.2470980G>A , CM000682.2:g.2470980G>A GRCh38
NC_000020.10:g.2451626G>A , CM000682.1:g.2451626G>A GRCh37
NC_000020.9:g.2399626G>A NCBI36
NG_042057.1:g.4874C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000461548.1:c.305-3222C>T ENSP00000456213.1:n.305-3222C>T