Canonical Allele Identifier: CA150690482
Gene:

Linked Data

dbSNP Id: rs965090659
gnomAD v2: 6-156133487-A-G
gnomAD v3: 6-155812353-A-G
gnomAD v4: 6-155812353-A-G
MyVariant Identifiers: chr6:g.156133487A>G (hg19) chr6:g.155812353A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812353A>G , CM000668.2:g.155812353A>G GRCh38
NC_000006.11:g.156133487A>G , CM000668.1:g.156133487A>G GRCh37
NC_000006.10:g.156175179A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+18934A>G
XR_943146.1:n.645-314T>C
XR_001744423.1:n.699-314T>C
XR_001744424.1:n.79+18934A>G
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