Canonical Allele Identifier: CA830285545

Gene:

Linked Data

• dbSNP Id: rs1218613043
• MyVariant Identifiers: chr6:g.98550291C>A (hg19) ; chr6:g.98102415C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98102415C>A , CM000668.2:g.98102415C>A	GRCh38
NC_000006.11:g.98550291C>A , CM000668.1:g.98550291C>A	GRCh37
NC_000006.10:g.98657012C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_245563.2:n.456+3145C>A
XR_942809.1:n.456+3145C>A