Canonical Allele Identifier: CA829017240
Gene:

Linked Data

dbSNP Id: rs1265447494
gnomAD v3: 6-8525166-G-A
gnomAD v4: 6-8525166-G-A
MyVariant Identifiers: chr6:g.8525399G>A (hg19) chr6:g.8525166G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8525166G>A , CM000668.2:g.8525166G>A GRCh38
NC_000006.11:g.8525399G>A , CM000668.1:g.8525399G>A GRCh37
NC_000006.10:g.8470398G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038979.1:n.626-33419G>A
NR_038980.1:n.649-33419G>A
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