Canonical Allele Identifier: CA151622552
Gene:

Linked Data

dbSNP Id: rs151023213

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.163765704C>T , CM000668.2:g.163765704C>T GRCh38
NC_000006.11:g.164186736C>T , CM000668.1:g.164186736C>T GRCh37
NC_000006.10:g.164106726C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001744452.1:n.410+6275C>T
XR_001744454.1:n.369+6316C>T
XR_001744455.1:n.346+6339C>T