Canonical Allele Identifier: CA150162954

Gene:

Linked Data

• dbSNP Id: rs956091298
• MyVariant Identifiers: chr6:g.151954801G>A (hg19) ; chr6:g.151633666G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151633666G>A , CM000668.2:g.151633666G>A	GRCh38
NC_000006.11:g.151954801G>A , CM000668.1:g.151954801G>A	GRCh37
NC_000006.10:g.151996494G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943115.1:n.2496+3684G>A