Canonical Allele Identifier: CA2611999003
Gene:

Linked Data

gnomAD v4: 11-2444546-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2444546C>T , CM000673.2:g.2444546C>T GRCh38
NC_000011.9:g.2465776C>T , CM000673.1:g.2465776C>T GRCh37
NC_000011.8:g.2422352C>T NCBI36
NG_008935.1:g.4556C>T , LRG_287:g.4556C>T

Transcript Alleles

HGVS Amino-acid Change
XR_930984.1:n.25G>A