Canonical Allele Identifier: CA310850359
Gene:

Linked Data

dbSNP Id: rs556430528
gnomAD v2: 20-2451666-C-T
gnomAD v3: 20-2471020-C-T
gnomAD v4: 20-2471020-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.2471020C>T , CM000682.2:g.2471020C>T GRCh38
NC_000020.10:g.2451666C>T , CM000682.1:g.2451666C>T GRCh37
NC_000020.9:g.2399666C>T NCBI36
NG_042057.1:g.4834G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000461548.1:c.305-3262G>A ENSP00000456213.1:n.305-3262G>A