Canonical Allele Identifier: CA823881836

Gene:

Linked Data

• dbSNP Id: rs1318056352
• MyVariant Identifiers: chr6:g.31407467G>A (hg19) ; chr6:g.31439690G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31439690G>A , CM000668.2:g.31439690G>A	GRCh38
NC_000006.11:g.31407467G>A , CM000668.1:g.31407467G>A	GRCh37
NC_000006.10:g.31515446G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_926694.1:n.417C>T