Canonical Allele Identifier: CA820836227

Gene:

Linked Data

• dbSNP Id: rs1342945959
• MyVariant Identifiers: chr6:g.151948368A>T (hg19) ; chr6:g.151627233A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151627233A>T , CM000668.2:g.151627233A>T	GRCh38
NC_000006.11:g.151948368A>T , CM000668.1:g.151948368A>T	GRCh37
NC_000006.10:g.151990061A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_943113.1:n.659A>T
XR_943115.1:n.659A>T