Canonical Allele Identifier: CA136858891

Gene:

Linked Data

• dbSNP Id: rs760401843
• MyVariant Identifiers: chr6:g.31407461T>G (hg19) ; chr6:g.31439684T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31439684T>G , CM000668.2:g.31439684T>G	GRCh38
NC_000006.11:g.31407461T>G , CM000668.1:g.31407461T>G	GRCh37
NC_000006.10:g.31515440T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_926694.1:n.423A>C