Canonical Allele Identifier: CA2651630778
Gene:

Linked Data

gnomAD v4: 20-2470995-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.2470995T>C , CM000682.2:g.2470995T>C GRCh38
NC_000020.10:g.2451641T>C , CM000682.1:g.2451641T>C GRCh37
NC_000020.9:g.2399641T>C NCBI36
NG_042057.1:g.4859A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000461548.1:c.305-3237A>G ENSP00000456213.1:n.305-3237A>G