Canonical Allele Identifier: CA306408650

Gene:

Linked Data

• dbSNP Id: rs921155498
• gnomAD v2: 19-20329277-C-A
• gnomAD v3: 19-20218468-C-A
• gnomAD v4: 19-20218468-C-A
• MyVariant Identifiers: chr19:g.20329277C>A (hg19) ; chr19:g.20218468C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.20218468C>A , CM000681.2:g.20218468C>A	GRCh38
NC_000019.9:g.20329277C>A , CM000681.1:g.20329277C>A	GRCh37
NC_000019.8:g.20190277C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_936388.1:n.619-1152G>T
XR_936389.1:n.502-1152G>T
XR_936390.1:n.511-1152G>T
XR_936391.1:n.514-1152G>T
XR_936392.1:n.514-1152G>T
XR_936394.1:n.41-266C>A
XR_001754063.2:n.1506-1152G>T
XR_001754064.2:n.138-1152G>T
XR_001754066.1:n.3912-1152G>T
XR_001754067.1:n.3912-1152G>T
XR_001754068.1:n.3912-1152G>T
XR_936394.2:n.41-266C>A
XR_936406.2:n.1411-1152G>T