Canonical Allele Identifier: CA16391117

Gene:

Linked Data

• dbSNP Id: rs10509091
• gnomAD v2: 10-60210790-T-G
• gnomAD v3: 10-58451030-T-G
• gnomAD v4: 10-58451030-T-G
• MyVariant Identifiers: chr10:g.60210790T>G (hg19) ; chr10:g.58451030T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.58451030T>G , CM000672.2:g.58451030T>G	GRCh38
NC_000010.10:g.60210790T>G , CM000672.1:g.60210790T>G	GRCh37
NC_000010.9:g.59880796T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_945981.1:n.356+15373T>G
XR_945982.1:n.356+15373T>G
XR_945983.1:n.356+15373T>G
XR_945984.1:n.113-16155T>G
XR_945985.1:n.73+14824T>G
XR_945986.1:n.356+15373T>G
XR_945981.2:n.360+15373T>G
XR_945982.2:n.360+15373T>G
XR_945983.2:n.360+15373T>G
XR_945984.2:n.117-16155T>G
XR_945985.2:n.73+14824T>G