Canonical Allele Identifier: CA569191027

Gene:

Linked Data

• dbSNP Id: rs1393627888
• gnomAD v2: 6-98550230-G-A
• gnomAD v3: 6-98102354-G-A
• gnomAD v4: 6-98102354-G-A
• MyVariant Identifiers: chr6:g.98550230G>A (hg19) ; chr6:g.98102354G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98102354G>A , CM000668.2:g.98102354G>A	GRCh38
NC_000006.11:g.98550230G>A , CM000668.1:g.98550230G>A	GRCh37
NC_000006.10:g.98656951G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_245563.2:n.456+3084G>A
XR_942809.1:n.456+3084G>A