Canonical Allele Identifier: CA2611999017
Gene:

Linked Data

gnomAD v4: 11-2444554-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2444554G>T , CM000673.2:g.2444554G>T GRCh38
NC_000011.9:g.2465784G>T , CM000673.1:g.2465784G>T GRCh37
NC_000011.8:g.2422360G>T NCBI36
NG_008935.1:g.4564G>T , LRG_287:g.4564G>T

Transcript Alleles

HGVS Amino-acid Change
XR_930984.1:n.17C>A