Canonical Allele Identifier: CA2327233074
Gene:

Linked Data

dbSNP Id: rs1773654250

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.20217991T>G , CM000681.2:g.20217991T>G GRCh38
NC_000019.9:g.20328800T>G , CM000681.1:g.20328800T>G GRCh37
NC_000019.8:g.20189800T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_936388.1:n.619-675A>C
XR_936389.1:n.502-675A>C
XR_936390.1:n.511-675A>C
XR_936391.1:n.514-675A>C
XR_936392.1:n.514-675A>C
XR_936394.1:n.41-743T>G
XR_001754063.2:n.1506-675A>C
XR_001754064.2:n.138-675A>C
XR_001754066.1:n.3912-675A>C
XR_001754067.1:n.3912-675A>C
XR_001754068.1:n.3912-675A>C
XR_936394.2:n.41-743T>G
XR_936406.2:n.1411-675A>C