Canonical Allele Identifier: CA134554886
Gene:

Linked Data

dbSNP Id: rs746009510
MyVariant Identifiers: chr6:g.8228925T>G (hg19) chr6:g.8228692T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8228692T>G , CM000668.2:g.8228692T>G GRCh38
NC_000006.11:g.8228925T>G , CM000668.1:g.8228925T>G GRCh37
NC_000006.10:g.8173924T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926440.1:n.83-1422T>G
XR_926441.1:n.190-10239T>G
XR_926442.1:n.83-1422T>G
XR_926443.1:n.83-10239T>G
XR_001743950.1:n.180-10239T>G
XR_926440.2:n.75-1422T>G
XR_926441.2:n.180-10239T>G
XR_926443.2:n.84-10239T>G
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