Canonical Allele Identifier: CA14708393

Gene:

Linked Data

• ClinVar Variation Id: 1239846
• ClinVar RCV Id: RCV001637810
• dbSNP Id: rs11878305
• gnomAD v2: 19-13049280-A-C
• gnomAD v3: 19-12938466-A-C
• gnomAD v4: 19-12938466-A-C
• COSMIC: COSN7354146
• MyVariant Identifiers: chr19:g.13049280A>C (hg19) ; chr19:g.12938466A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12938466A>C , CM000681.2:g.12938466A>C	GRCh38
NC_000019.9:g.13049280A>C , CM000681.1:g.13049280A>C	GRCh37
NC_000019.8:g.12910280A>C	NCBI36
NG_029662.1:g.4867A>C , LRG_828:g.4867A>C