Canonical Allele Identifier: CA595462965

Gene:

Linked Data

• dbSNP Id: rs1472219556
• gnomAD v2: 10-101861461-C-G
• gnomAD v3: 10-100101704-C-G
• gnomAD v4: 10-100101704-C-G
• MyVariant Identifiers: chr10:g.101861461C>G (hg19) ; chr10:g.100101704C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100101704C>G , CM000672.2:g.100101704C>G	GRCh38
NC_000010.10:g.101861461C>G , CM000672.1:g.101861461C>G	GRCh37
NC_000010.9:g.101851451C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_946245.1:n.185+5467C>G