Canonical Allele Identifier: CA144319790

Gene:

Linked Data

• dbSNP Id: rs1044842967
• MyVariant Identifiers: chr6:g.98550362A>G (hg19) ; chr6:g.98102486A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98102486A>G , CM000668.2:g.98102486A>G	GRCh38
NC_000006.11:g.98550362A>G , CM000668.1:g.98550362A>G	GRCh37
NC_000006.10:g.98657083A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_245563.2:n.456+3216A>G
XR_942809.1:n.456+3216A>G