Canonical Allele Identifier: CA212877311

Gene:

Linked Data

• dbSNP Id: rs564205770
• gnomAD v2: 10-101861490-G-A
• gnomAD v3: 10-100101733-G-A
• gnomAD v4: 10-100101733-G-A
• MyVariant Identifiers: chr10:g.101861490G>A (hg19) ; chr10:g.100101733G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100101733G>A , CM000672.2:g.100101733G>A	GRCh38
NC_000010.10:g.101861490G>A , CM000672.1:g.101861490G>A	GRCh37
NC_000010.9:g.101851480G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_946245.1:n.185+5496G>A