Canonical Allele Identifier: CA830248092
Gene:

Linked Data

dbSNP Id: rs1164784495
gnomAD v3: 6-98048121-T-A
gnomAD v4: 6-98048121-T-A
MyVariant Identifiers: chr6:g.98495997T>A (hg19) chr6:g.98048121T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98048121T>A , CM000668.2:g.98048121T>A GRCh38
NC_000006.11:g.98495997T>A , CM000668.1:g.98495997T>A GRCh37
NC_000006.10:g.98602718T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.372-51065T>A
XR_942809.1:n.372-51065T>A
Search 100 bp 5'
Search 100 bp 3'