Canonical Allele Identifier: CA134548256
Gene:

Linked Data

dbSNP Id: rs922166090
MyVariant Identifiers: chr6:g.8169765T>C (hg19) chr6:g.8169532T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8169532T>C , CM000668.2:g.8169532T>C GRCh38
NC_000006.11:g.8169765T>C , CM000668.1:g.8169765T>C GRCh37
NC_000006.10:g.8114764T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926440.1:n.82+11272T>C
XR_926441.1:n.189+1612T>C
XR_926442.1:n.82+11272T>C
XR_926443.1:n.82+11272T>C
XR_001743950.1:n.179+1612T>C
XR_926440.2:n.74+11272T>C
XR_926441.2:n.179+1612T>C
XR_926443.2:n.83+11272T>C
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