Canonical Allele Identifier: CA144309873

Gene:

Linked Data

• dbSNP Id: rs941966878
• MyVariant Identifiers: chr6:g.98462379C>G (hg19) ; chr6:g.98014503C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98014503C>G , CM000668.2:g.98014503C>G	GRCh38
NC_000006.11:g.98462379C>G , CM000668.1:g.98462379C>G	GRCh37
NC_000006.10:g.98569100C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_245563.2:n.371+45037C>G
XR_942809.1:n.371+45037C>G