Canonical Allele Identifier: CA305512629

Gene:

Linked Data

• ClinVar Variation Id: 3048325
• ClinVar RCV Id: RCV003952098
• dbSNP Id: rs757911363
• gnomAD v2: 19-13049211-C-A
• gnomAD v3: 19-12938397-C-A
• gnomAD v4: 19-12938397-C-A
• MyVariant Identifiers: chr19:g.13049211C>A (hg19) ; chr19:g.12938397C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12938397C>A , CM000681.2:g.12938397C>A	GRCh38
NC_000019.9:g.13049211C>A , CM000681.1:g.13049211C>A	GRCh37
NC_000019.8:g.12910211C>A	NCBI36
NG_029662.1:g.4798C>A , LRG_828:g.4798C>A