Canonical Allele Identifier: CA98367529

Gene:

Linked Data

• dbSNP Id: rs963437325
• gnomAD v2: 4-63423717-G-A
• gnomAD v3: 4-62557999-G-A
• gnomAD v4: 4-62557999-G-A
• MyVariant Identifiers: chr4:g.63423717G>A (hg19) ; chr4:g.62557999G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.62557999G>A , CM000666.2:g.62557999G>A	GRCh38
NC_000004.11:g.63423717G>A , CM000666.1:g.63423717G>A	GRCh37
NC_000004.10:g.63106312G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_938814.1:n.161-5845G>A