Canonical Allele Identifier: CA230606004
Gene:

Linked Data

dbSNP Id: rs79973597
gnomAD v2: 11-128740824-G-C
gnomAD v3: 11-128870929-G-C
gnomAD v4: 11-128870929-G-C
MyVariant Identifiers: chr11:g.128740824G>C (hg19) chr11:g.128870929G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128870929G>C , CM000673.2:g.128870929G>C GRCh38
NC_000011.9:g.128740824G>C , CM000673.1:g.128740824G>C GRCh37
NC_000011.8:g.128246034G>C NCBI36
NG_009379.1:g.1445C>G

Transcript Alleles

HGVS Amino-acid Change
XR_948172.1:n.5982C>G
XR_948173.1:n.5671C>G
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