Canonical Allele Identifier: CA821223581
Gene:

Linked Data

dbSNP Id: rs184212863
gnomAD v3: 6-155812456-C-A
gnomAD v4: 6-155812456-C-A
MyVariant Identifiers: chr6:g.156133590C>A (hg19) chr6:g.155812456C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812456C>A , CM000668.2:g.155812456C>A GRCh38
NC_000006.11:g.156133590C>A , CM000668.1:g.156133590C>A GRCh37
NC_000006.10:g.156175282C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+19037C>A
XR_943146.1:n.645-417G>T
XR_001744423.1:n.699-417G>T
XR_001744424.1:n.79+19037C>A
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