Canonical Allele Identifier: CA602368385
Gene:

Linked Data

dbSNP Id: rs1354365711
gnomAD v2: 11-128740843-C-G
gnomAD v3: 11-128870948-C-G
gnomAD v4: 11-128870948-C-G
MyVariant Identifiers: chr11:g.128740843C>G (hg19) chr11:g.128870948C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128870948C>G , CM000673.2:g.128870948C>G GRCh38
NC_000011.9:g.128740843C>G , CM000673.1:g.128740843C>G GRCh37
NC_000011.8:g.128246053C>G NCBI36
NG_009379.1:g.1426G>C

Transcript Alleles

HGVS Amino-acid Change
XR_948172.1:n.5963G>C
XR_948173.1:n.5652G>C
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