Canonical Allele Identifier: CA2726809125
Gene:

Linked Data

dbSNP Id: rs2120874761

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.84951996T>C , CM000674.2:g.84951996T>C GRCh38
NC_000012.11:g.85345775T>C , CM000674.1:g.85345775T>C GRCh37
NC_000012.10:g.83869906T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945152.1:n.316+30682T>C
XR_945153.1:n.301+13532T>C
XR_945154.1:n.175-36946T>C
XR_945155.1:n.330+30682T>C
XR_945152.2:n.316+30682T>C
XR_945154.2:n.175-36946T>C
XR_945155.2:n.888+30682T>C