Canonical Allele Identifier: CA151622550
Gene:

Linked Data

dbSNP Id: rs528503625

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.163765665T>C , CM000668.2:g.163765665T>C GRCh38
NC_000006.11:g.164186697T>C , CM000668.1:g.164186697T>C GRCh37
NC_000006.10:g.164106687T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001744452.1:n.410+6236T>C
XR_001744454.1:n.369+6277T>C
XR_001744455.1:n.346+6300T>C