Canonical Allele Identifier: CA820836171

Gene:

Linked Data

• dbSNP Id: rs1358045712
• MyVariant Identifiers: chr6:g.151948269G>A (hg19) ; chr6:g.151627134G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151627134G>A , CM000668.2:g.151627134G>A	GRCh38
NC_000006.11:g.151948269G>A , CM000668.1:g.151948269G>A	GRCh37
NC_000006.10:g.151989962G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_943113.1:n.560G>A
XR_943115.1:n.560G>A