Canonical Allele Identifier: CA144319779

Gene:

Linked Data

• dbSNP Id: rs934691597
• MyVariant Identifiers: chr6:g.98102439C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98102439C>A , CM000668.2:g.98102439C>A	GRCh38
NC_000006.11:g.98550315C>A , CM000668.1:g.98550315C>A	GRCh37
NC_000006.10:g.98657036C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_245563.2:n.456+3169C>A
XR_942809.1:n.456+3169C>A