Canonical Allele Identifier: CA2327233213
Gene:

Linked Data

dbSNP Id: rs1599734113

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.20218285T>C , CM000681.2:g.20218285T>C GRCh38
NC_000019.9:g.20329094T>C , CM000681.1:g.20329094T>C GRCh37
NC_000019.8:g.20190094T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_936388.1:n.619-969A>G
XR_936389.1:n.502-969A>G
XR_936390.1:n.511-969A>G
XR_936391.1:n.514-969A>G
XR_936392.1:n.514-969A>G
XR_936394.1:n.41-449T>C
XR_001754063.2:n.1506-969A>G
XR_001754064.2:n.138-969A>G
XR_001754066.1:n.3912-969A>G
XR_001754067.1:n.3912-969A>G
XR_001754068.1:n.3912-969A>G
XR_936394.2:n.41-449T>C
XR_936406.2:n.1411-969A>G