Canonical Allele Identifier: CA2611998991
Gene:

Linked Data

gnomAD v4: 11-2444535-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2444535C>T , CM000673.2:g.2444535C>T GRCh38
NC_000011.9:g.2465765C>T , CM000673.1:g.2465765C>T GRCh37
NC_000011.8:g.2422341C>T NCBI36
NG_008935.1:g.4545C>T , LRG_287:g.4545C>T

Transcript Alleles

HGVS Amino-acid Change
XR_930984.1:n.36G>A
Search 100 bp 5'
Search 100 bp 3'