Canonical Allele Identifier: CA830248085
Gene:

Linked Data

dbSNP Id: rs1422610870
MyVariant Identifiers: chr6:g.98495991C>A (hg19) chr6:g.98048115C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98048115C>A , CM000668.2:g.98048115C>A GRCh38
NC_000006.11:g.98495991C>A , CM000668.1:g.98495991C>A GRCh37
NC_000006.10:g.98602712C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245563.2:n.372-51071C>A
XR_942809.1:n.372-51071C>A
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