Canonical Allele Identifier: CA816711658
Gene:

Linked Data

dbSNP Id: rs1201467840
MyVariant Identifiers: chr6:g.106253018G>A (hg19) chr6:g.105805143G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.105805143G>A , CM000668.2:g.105805143G>A GRCh38
NC_000006.11:g.106253018G>A , CM000668.1:g.106253018G>A GRCh37
NC_000006.10:g.106359711G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_942835.1:n.510+24914C>T
XR_001744274.1:n.438+24914C>T
XR_001744275.1:n.337+24914C>T
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