Canonical Allele Identifier: CA1888525178
Gene:

Linked Data

dbSNP Id: rs1588679902

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.7047069A>G , CM000672.2:g.7047069A>G GRCh38
NC_000010.10:g.7089031A>G , CM000672.1:g.7089031A>G GRCh37
NC_000010.9:g.7129037A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930623.1:n.173-16752T>C
XR_930624.1:n.171-16752T>C
XR_930625.1:n.172-16752T>C
XR_930626.1:n.168-16752T>C
XR_930627.1:n.173-16752T>C
XR_001747351.1:n.364-16752T>C
XR_001747352.1:n.364-16752T>C
XR_001747353.1:n.188-34413T>C
XR_001747354.1:n.364-16752T>C
XR_930623.2:n.364-16752T>C
XR_930624.2:n.364-16752T>C
XR_930625.2:n.364-16752T>C
XR_930626.2:n.364-16752T>C
XR_930627.2:n.364-16752T>C