Canonical Allele Identifier: CA673239405
Gene:

Linked Data

dbSNP Id: rs1408723522
gnomAD v3: 11-128455459-C-T
gnomAD v4: 11-128455459-C-T
MyVariant Identifiers: chr11:g.128325354C>T (hg19) chr11:g.128455459C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128455459C>T , CM000673.2:g.128455459C>T GRCh38
NC_000011.9:g.128325354C>T , CM000673.1:g.128325354C>T GRCh37
NC_000011.8:g.127830564C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948164.1:n.4179C>T
XR_948165.1:n.3467+712C>T
Search 100 bp 5'
Search 100 bp 3'