Canonical Allele Identifier: CA144313441
Gene:

Linked Data

dbSNP Id: rs915946124
MyVariant Identifiers: chr6:g.98495971T>A (hg19) chr6:g.98048095T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98048095T>A , CM000668.2:g.98048095T>A GRCh38
NC_000006.11:g.98495971T>A , CM000668.1:g.98495971T>A GRCh37
NC_000006.10:g.98602692T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.372-51091T>A
XR_942809.1:n.372-51091T>A
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Search 100 bp 3'