Canonical Allele Identifier: CA208046113

Gene:

Linked Data

• dbSNP Id: rs7085387
• gnomAD v2: 10-60204602-G-A
• gnomAD v3: 10-58444842-G-A
• gnomAD v4: 10-58444842-G-A
• MyVariant Identifiers: chr10:g.60204602G>A (hg19) ; chr10:g.58444842G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.58444842G>A , CM000672.2:g.58444842G>A	GRCh38
NC_000010.10:g.60204602G>A , CM000672.1:g.60204602G>A	GRCh37
NC_000010.9:g.59874608G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_945981.1:n.356+9185G>A
XR_945982.1:n.356+9185G>A
XR_945983.1:n.356+9185G>A
XR_945984.1:n.112+10801G>A
XR_945985.1:n.73+8636G>A
XR_945986.1:n.356+9185G>A
XR_945981.2:n.360+9185G>A
XR_945982.2:n.360+9185G>A
XR_945983.2:n.360+9185G>A
XR_945984.2:n.116+10801G>A
XR_945985.2:n.73+8636G>A