Canonical Allele Identifier: CA136859078

Gene:

Linked Data

• dbSNP Id: rs749775773
• MyVariant Identifiers: chr6:g.31407797T>A (hg19) ; chr6:g.31440020T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31440020T>A , CM000668.2:g.31440020T>A	GRCh38
NC_000006.11:g.31407797T>A , CM000668.1:g.31407797T>A	GRCh37
NC_000006.10:g.31515776T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_926694.1:n.87A>T