Canonical Allele Identifier: CA829017259
Gene:

Linked Data

dbSNP Id: rs1388382701
MyVariant Identifiers: chr6:g.8525442A>C (hg19) chr6:g.8525209A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8525209A>C , CM000668.2:g.8525209A>C GRCh38
NC_000006.11:g.8525442A>C , CM000668.1:g.8525442A>C GRCh37
NC_000006.10:g.8470441A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038979.1:n.626-33376A>C
NR_038980.1:n.649-33376A>C
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