Canonical Allele Identifier: CA2651630711
Gene:

Linked Data

gnomAD v4: 20-2470918-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.2470918G>T , CM000682.2:g.2470918G>T GRCh38
NC_000020.10:g.2451564G>T , CM000682.1:g.2451564G>T GRCh37
NC_000020.9:g.2399564G>T NCBI36
NG_042057.1:g.4936C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000461548.1:c.305-3160C>A ENSP00000456213.1:n.305-3160C>A