Canonical Allele Identifier: CA2327233305

Gene:

Linked Data

• dbSNP Id: rs965209718

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.20218459G>C , CM000681.2:g.20218459G>C	GRCh38
NC_000019.9:g.20329268G>C , CM000681.1:g.20329268G>C	GRCh37
NC_000019.8:g.20190268G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_936388.1:n.619-1143C>G
XR_936389.1:n.502-1143C>G
XR_936390.1:n.511-1143C>G
XR_936391.1:n.514-1143C>G
XR_936392.1:n.514-1143C>G
XR_936394.1:n.41-275G>C
XR_001754063.2:n.1506-1143C>G
XR_001754064.2:n.138-1143C>G
XR_001754066.1:n.3912-1143C>G
XR_001754067.1:n.3912-1143C>G
XR_001754068.1:n.3912-1143C>G
XR_936394.2:n.41-275G>C
XR_936406.2:n.1411-1143C>G