Canonical Allele Identifier: CA171706560
Gene:

Linked Data

dbSNP Id: rs1038597174
MyVariant Identifiers: chr8:g.5765326C>G (hg19) chr8:g.5907804C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.5907804C>G , CM000670.2:g.5907804C>G GRCh38
NC_000008.10:g.5765326C>G , CM000670.1:g.5765326C>G GRCh37
NC_000008.9:g.5752734C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_941374.1:n.308-8073G>C
XR_941375.1:n.308-8073G>C
XR_941376.1:n.406-8073G>C
XR_941377.1:n.308-8073G>C
XR_941378.1:n.216-8073G>C
XR_001745765.1:n.308-8073G>C
XR_001745766.1:n.406-8073G>C
XR_001745767.1:n.216-8073G>C
XR_001745768.1:n.308-8073G>C
XR_941374.2:n.308-8073G>C
XR_941375.2:n.308-8073G>C
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