Canonical Allele Identifier: CA880474175

Gene:

Linked Data

• dbSNP Id: rs1380646999
• gnomAD v3: 19-20217888-T-C
• gnomAD v4: 19-20217888-T-C
• MyVariant Identifiers: chr19:g.20217888T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.20217888T>C , CM000681.2:g.20217888T>C	GRCh38
NC_000019.9:g.20328697T>C , CM000681.1:g.20328697T>C	GRCh37
NC_000019.8:g.20189697T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_936388.1:n.619-572A>G
XR_936389.1:n.502-572A>G
XR_936390.1:n.511-572A>G
XR_936391.1:n.514-572A>G
XR_936392.1:n.514-572A>G
XR_936394.1:n.41-846T>C
XR_001754063.2:n.1506-572A>G
XR_001754064.2:n.138-572A>G
XR_001754066.1:n.3912-572A>G
XR_001754067.1:n.3912-572A>G
XR_001754068.1:n.3912-572A>G
XR_936394.2:n.41-846T>C
XR_936406.2:n.1411-572A>G