Canonical Allele Identifier: CA171706515
Gene:

Linked Data

dbSNP Id: rs569661386
gnomAD v2: 8-5765142-C-G
gnomAD v3: 8-5907620-C-G
gnomAD v4: 8-5907620-C-G
MyVariant Identifiers: chr8:g.5765142C>G (hg19) chr8:g.5907620C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.5907620C>G , CM000670.2:g.5907620C>G GRCh38
NC_000008.10:g.5765142C>G , CM000670.1:g.5765142C>G GRCh37
NC_000008.9:g.5752550C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_941374.1:n.308-7889G>C
XR_941375.1:n.308-7889G>C
XR_941376.1:n.406-7889G>C
XR_941377.1:n.308-7889G>C
XR_941378.1:n.216-7889G>C
XR_001745765.1:n.308-7889G>C
XR_001745766.1:n.406-7889G>C
XR_001745767.1:n.216-7889G>C
XR_001745768.1:n.308-7889G>C
XR_941374.2:n.308-7889G>C
XR_941375.2:n.308-7889G>C
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