Canonical Allele Identifier: CA602555872
Gene:

Linked Data

dbSNP Id: rs1175891755
gnomAD v2: 11-128325430-T-C
gnomAD v3: 11-128455535-T-C
gnomAD v4: 11-128455535-T-C
MyVariant Identifiers: chr11:g.128325430T>C (hg19) chr11:g.128455535T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128455535T>C , CM000673.2:g.128455535T>C GRCh38
NC_000011.9:g.128325430T>C , CM000673.1:g.128325430T>C GRCh37
NC_000011.8:g.127830640T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948164.1:n.4255T>C
XR_948165.1:n.3467+788T>C
Search 100 bp 5'
Search 100 bp 3'