Canonical Allele Identifier: CA821223449
Gene:

Linked Data

dbSNP Id: rs1427003427
gnomAD v3: 6-155812235-G-A
gnomAD v4: 6-155812235-G-A
MyVariant Identifiers: chr6:g.156133369G>A (hg19) chr6:g.155812235G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812235G>A , CM000668.2:g.155812235G>A GRCh38
NC_000006.11:g.156133369G>A , CM000668.1:g.156133369G>A GRCh37
NC_000006.10:g.156175061G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+18816G>A
XR_943146.1:n.645-196C>T
XR_001744423.1:n.699-196C>T
XR_001744424.1:n.79+18816G>A
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