Canonical Allele Identifier: CA829017257
Gene:

Linked Data

dbSNP Id: rs1321361412
MyVariant Identifiers: chr6:g.8525439G>A (hg19) chr6:g.8525206G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8525206G>A , CM000668.2:g.8525206G>A GRCh38
NC_000006.11:g.8525439G>A , CM000668.1:g.8525439G>A GRCh37
NC_000006.10:g.8470438G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038979.1:n.626-33379G>A
NR_038980.1:n.649-33379G>A
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