Canonical Allele Identifier: CA828661954
Gene:

Linked Data

dbSNP Id: rs762705109
gnomAD v3: 6-8169753-G-C
gnomAD v4: 6-8169753-G-C
MyVariant Identifiers: chr6:g.8169986G>C (hg19) chr6:g.8169753G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8169753G>C , CM000668.2:g.8169753G>C GRCh38
NC_000006.11:g.8169986G>C , CM000668.1:g.8169986G>C GRCh37
NC_000006.10:g.8114985G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926440.1:n.82+11493G>C
XR_926441.1:n.189+1833G>C
XR_926442.1:n.82+11493G>C
XR_926443.1:n.82+11493G>C
XR_001743950.1:n.179+1833G>C
XR_926440.2:n.74+11493G>C
XR_926441.2:n.179+1833G>C
XR_926443.2:n.83+11493G>C
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