Canonical Allele Identifier: CA1096188007
Gene:

Linked Data

dbSNP Id: rs1778853430
gnomAD v3: 6-155812260-T-A
gnomAD v4: 6-155812260-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812260T>A , CM000668.2:g.155812260T>A GRCh38
NC_000006.11:g.156133394T>A , CM000668.1:g.156133394T>A GRCh37
NC_000006.10:g.156175086T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+18841T>A
XR_943146.1:n.645-221A>T
XR_001744423.1:n.699-221A>T
XR_001744424.1:n.79+18841T>A
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