Canonical Allele Identifier: CA230606029
Gene:

Linked Data

dbSNP Id: rs919107916
gnomAD v2: 11-128740863-A-C
gnomAD v3: 11-128870968-A-C
gnomAD v4: 11-128870968-A-C
MyVariant Identifiers: chr11:g.128740863A>C (hg19) chr11:g.128870968A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128870968A>C , CM000673.2:g.128870968A>C GRCh38
NC_000011.9:g.128740863A>C , CM000673.1:g.128740863A>C GRCh37
NC_000011.8:g.128246073A>C NCBI36
NG_009379.1:g.1406T>G

Transcript Alleles

HGVS Amino-acid Change
XR_948172.1:n.5943T>G
XR_948173.1:n.5632T>G
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Search 100 bp 3'