Canonical Allele Identifier: CA99746702

Gene:

Linked Data

• dbSNP Id: rs746560409
• gnomAD v3: 4-74304431-A-G
• gnomAD v4: 4-74304431-A-G
• MyVariant Identifiers: chr4:g.75170148A>G (hg19) ; chr4:g.74304431A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.74304431A>G , CM000666.2:g.74304431A>G	GRCh38
NC_000004.11:g.75170148A>G , CM000666.1:g.75170148A>G	GRCh37
NC_000004.10:g.75389012A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_938877.1:n.120-25653T>C
XR_938877.2:n.126-25653T>C