Canonical Allele Identifier: CA230605967
Gene:

Linked Data

dbSNP Id: rs117769244
gnomAD v2: 11-128740727-C-A
gnomAD v3: 11-128870832-C-A
gnomAD v4: 11-128870832-C-A
MyVariant Identifiers: chr11:g.128740727C>A (hg19) chr11:g.128870832C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128870832C>A , CM000673.2:g.128870832C>A GRCh38
NC_000011.9:g.128740727C>A , CM000673.1:g.128740727C>A GRCh37
NC_000011.8:g.128245937C>A NCBI36
NG_009379.1:g.1542G>T

Transcript Alleles

HGVS Amino-acid Change
XR_948172.1:n.6079G>T
XR_948173.1:n.5768G>T
Search 100 bp 5'
Search 100 bp 3'