Canonical Allele Identifier: CA823881850

Gene:

Linked Data

• dbSNP Id: rs1323862755
• MyVariant Identifiers: chr6:g.31407479G>A (hg19) ; chr6:g.31439702G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31439702G>A , CM000668.2:g.31439702G>A	GRCh38
NC_000006.11:g.31407479G>A , CM000668.1:g.31407479G>A	GRCh37
NC_000006.10:g.31515458G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_926694.1:n.405C>T