Canonical Allele Identifier: CA1096188034
Gene:

Linked Data

dbSNP Id: rs1778854945
gnomAD v3: 6-155812368-T-G
gnomAD v4: 6-155812368-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812368T>G , CM000668.2:g.155812368T>G GRCh38
NC_000006.11:g.156133502T>G , CM000668.1:g.156133502T>G GRCh37
NC_000006.10:g.156175194T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+18949T>G
XR_943146.1:n.645-329A>C
XR_001744423.1:n.699-329A>C
XR_001744424.1:n.79+18949T>G
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