Canonical Allele Identifier: CA224796468
Gene:

Linked Data

dbSNP Id: rs147269019
gnomAD v2: 11-76465781-G-C
gnomAD v3: 11-76754737-G-C
gnomAD v4: 11-76754737-G-C
MyVariant Identifiers: chr11:g.76465781G>C (hg19) chr11:g.76754737G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.76754737G>C , CM000673.2:g.76754737G>C GRCh38
NC_000011.9:g.76465781G>C , CM000673.1:g.76465781G>C GRCh37
NC_000011.8:g.76143429G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_950336.1:n.418+1633G>C
XR_950337.1:n.418+1633G>C
XR_950336.2:n.510+1633G>C
XR_950337.2:n.508+1633G>C
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