Canonical Allele Identifier: CA150690478
Gene:

Linked Data

dbSNP Id: rs769241177
gnomAD v3: 6-155812325-C-T
gnomAD v4: 6-155812325-C-T
MyVariant Identifiers: chr6:g.156133459C>T (hg19) chr6:g.155812325C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812325C>T , CM000668.2:g.155812325C>T GRCh38
NC_000006.11:g.156133459C>T , CM000668.1:g.156133459C>T GRCh37
NC_000006.10:g.156175151C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+18906C>T
XR_943146.1:n.645-286G>A
XR_001744423.1:n.699-286G>A
XR_001744424.1:n.79+18906C>T
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