Canonical Allele Identifier: CA13201214

Gene:

Linked Data

• dbSNP Id: rs79871907
• gnomAD v2: 10-101861438-G-A
• gnomAD v3: 10-100101681-G-A
• gnomAD v4: 10-100101681-G-A
• MyVariant Identifiers: chr10:g.101861438G>A (hg19) ; chr10:g.100101681G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100101681G>A , CM000672.2:g.100101681G>A	GRCh38
NC_000010.10:g.101861438G>A , CM000672.1:g.101861438G>A	GRCh37
NC_000010.9:g.101851428G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_946245.1:n.185+5444G>A