Canonical Allele Identifier: CA823881952

Gene:

Linked Data

• dbSNP Id: rs1489958228
• MyVariant Identifiers: chr6:g.31407710G>A (hg19) ; chr6:g.31439933G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31439933G>A , CM000668.2:g.31439933G>A	GRCh38
NC_000006.11:g.31407710G>A , CM000668.1:g.31407710G>A	GRCh37
NC_000006.10:g.31515689G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_926694.1:n.174C>T