Canonical Allele Identifier: CA104732932

Gene:

Linked Data

• dbSNP Id: rs1038559409
• gnomAD v2: 4-122619831-C-T
• gnomAD v3: 4-121698676-C-T
• gnomAD v4: 4-121698676-C-T
• MyVariant Identifiers: chr4:g.122619831C>T (hg19) ; chr4:g.121698676C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121698676C>T , CM000666.2:g.121698676C>T	GRCh38
NC_000004.11:g.122619831C>T , CM000666.1:g.122619831C>T	GRCh37
NC_000004.10:g.122839281C>T	NCBI36
NG_032042.1:g.3317G>A