Canonical Allele Identifier: CA830285599
Gene:

Linked Data

dbSNP Id: rs1451716845
MyVariant Identifiers: chr6:g.98550338A>C (hg19) chr6:g.98102462A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98102462A>C , CM000668.2:g.98102462A>C GRCh38
NC_000006.11:g.98550338A>C , CM000668.1:g.98550338A>C GRCh37
NC_000006.10:g.98657059A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245563.2:n.456+3192A>C
XR_942809.1:n.456+3192A>C
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