Canonical Allele Identifier: CA310144744

Gene:

Linked Data

• ClinVar Variation Id: 1209416
• ClinVar RCV Id: RCV001578068
• dbSNP Id: rs143032168
• gnomAD v2: 19-55663096-G-T
• gnomAD v3: 19-55151728-G-T
• gnomAD v4: 19-55151728-G-T
• MyVariant Identifiers: chr19:g.55663096G>T (hg19) ; chr19:g.55151728G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55151728G>T , CM000681.2:g.55151728G>T	GRCh38
NC_000019.9:g.55663096G>T , CM000681.1:g.55663096G>T	GRCh37
NC_000019.8:g.60354908G>T	NCBI36
NG_007866.2:g.11005C>A , LRG_432:g.11005C>A
NG_011829.2:g.2511C>A