Canonical Allele Identifier: CA825142432

Gene:

Linked Data

• dbSNP Id: rs1425245890
• gnomAD v3: 6-465819-G-A
• gnomAD v4: 6-465819-G-A
• MyVariant Identifiers: chr6:g.465819G>A (hg19) ; chr6:g.465819G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.465819G>A , CM000668.2:g.465819G>A	GRCh38
NC_000006.11:g.465819G>A , CM000668.1:g.465819G>A	GRCh37
NC_000006.10:g.410819G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_926364.1:n.2714+12094G>A
XR_926365.1:n.2548+12094G>A
XR_001743914.1:n.482-9389G>A