Canonical Allele Identifier: CA2346122721
Gene:

Linked Data

dbSNP Id: rs2085111079
gnomAD v4: 20-2470871-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.2470871C>T , CM000682.2:g.2470871C>T GRCh38
NC_000020.10:g.2451517C>T , CM000682.1:g.2451517C>T GRCh37
NC_000020.9:g.2399517C>T NCBI36
NG_042057.1:g.4983G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000461548.1:c.305-3113G>A ENSP00000456213.1:n.305-3113G>A