Canonical Allele Identifier: CA2651630781
Gene:

Linked Data

gnomAD v4: 20-2470999-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.2470999A>T , CM000682.2:g.2470999A>T GRCh38
NC_000020.10:g.2451645A>T , CM000682.1:g.2451645A>T GRCh37
NC_000020.9:g.2399645A>T NCBI36
NG_042057.1:g.4855T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000461548.1:c.305-3241T>A ENSP00000456213.1:n.305-3241T>A