Canonical Allele Identifier: CA830248062
Gene:

Linked Data

dbSNP Id: rs1372793069
MyVariant Identifiers: chr6:g.98495959A>G (hg19) chr6:g.98048083A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98048083A>G , CM000668.2:g.98048083A>G GRCh38
NC_000006.11:g.98495959A>G , CM000668.1:g.98495959A>G GRCh37
NC_000006.10:g.98602680A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.372-51103A>G
XR_942809.1:n.372-51103A>G
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