Canonical Allele Identifier: CA566344775
Gene:

Linked Data

dbSNP Id: rs1308695708
gnomAD v2: 6-31407899-C-T
gnomAD v3: 6-31440122-C-T
gnomAD v4: 6-31440122-C-T
MyVariant Identifiers: chr6:g.31407899C>T (hg19) chr6:g.31440122C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31440122C>T , CM000668.2:g.31440122C>T GRCh38
NC_000006.11:g.31407899C>T , CM000668.1:g.31407899C>T GRCh37
NC_000006.10:g.31515878C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926694.1:n.55-70G>A
Search 100 bp 5'
Search 100 bp 3'