Canonical Allele Identifier: CA816711673
Gene:

Linked Data

dbSNP Id: rs1310106554
MyVariant Identifiers: chr6:g.106253031T>A (hg19) chr6:g.105805156T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.105805156T>A , CM000668.2:g.105805156T>A GRCh38
NC_000006.11:g.106253031T>A , CM000668.1:g.106253031T>A GRCh37
NC_000006.10:g.106359724T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_942835.1:n.510+24901A>T
XR_001744274.1:n.438+24901A>T
XR_001744275.1:n.337+24901A>T
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