Canonical Allele Identifier: CA105096494

Gene:

Linked Data

• dbSNP Id: rs555976820
• gnomAD v2: 4-121513190-C-T
• gnomAD v3: 4-120592035-C-T
• gnomAD v4: 4-120592035-C-T
• MyVariant Identifiers: chr4:g.121513190C>T (hg19) ; chr4:g.120592035C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.120592035C>T , CM000666.2:g.120592035C>T	GRCh38
NC_000004.11:g.121513190C>T , CM000666.1:g.121513190C>T	GRCh37
NC_000004.10:g.121732640C>T	NCBI36