Canonical Allele Identifier: CA798354176

Gene:

Linked Data

• dbSNP Id: rs1411389598
• gnomAD v3: 4-74304404-T-A
• gnomAD v4: 4-74304404-T-A
• MyVariant Identifiers: chr4:g.75170121T>A (hg19) ; chr4:g.74304404T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.74304404T>A , CM000666.2:g.74304404T>A	GRCh38
NC_000004.11:g.75170121T>A , CM000666.1:g.75170121T>A	GRCh37
NC_000004.10:g.75388985T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_938877.1:n.120-25626A>T
XR_938877.2:n.126-25626A>T