Canonical Allele Identifier: CA880474147

Gene:

Linked Data

• dbSNP Id: rs1437116255
• gnomAD v3: 19-20217873-T-C
• gnomAD v4: 19-20217873-T-C
• MyVariant Identifiers: chr19:g.20217873T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.20217873T>C , CM000681.2:g.20217873T>C	GRCh38
NC_000019.9:g.20328682T>C , CM000681.1:g.20328682T>C	GRCh37
NC_000019.8:g.20189682T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_936388.1:n.619-557A>G
XR_936389.1:n.502-557A>G
XR_936390.1:n.511-557A>G
XR_936391.1:n.514-557A>G
XR_936392.1:n.514-557A>G
XR_936394.1:n.41-861T>C
XR_001754063.2:n.1506-557A>G
XR_001754064.2:n.138-557A>G
XR_001754066.1:n.3912-557A>G
XR_001754067.1:n.3912-557A>G
XR_001754068.1:n.3912-557A>G
XR_936394.2:n.41-861T>C
XR_936406.2:n.1411-557A>G