Canonical Allele Identifier: CA830285574

Gene:

Linked Data

• dbSNP Id: rs895929809
• MyVariant Identifiers: chr6:g.98550324T>C (hg19) ; chr6:g.98102448T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98102448T>C , CM000668.2:g.98102448T>C	GRCh38
NC_000006.11:g.98550324T>C , CM000668.1:g.98550324T>C	GRCh37
NC_000006.10:g.98657045T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_245563.2:n.456+3178T>C
XR_942809.1:n.456+3178T>C