Canonical Allele Identifier: CA1092269837

Gene:

Linked Data

• dbSNP Id: rs1773159420
• gnomAD v3: 6-98102432-T-A
• gnomAD v4: 6-98102432-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98102432T>A , CM000668.2:g.98102432T>A	GRCh38
NC_000006.11:g.98550308T>A , CM000668.1:g.98550308T>A	GRCh37
NC_000006.10:g.98657029T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_245563.2:n.456+3162T>A
XR_942809.1:n.456+3162T>A