Canonical Allele Identifier: CA1678638509
Gene:

Linked Data

dbSNP Id: rs1431978306

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.163765683T>G , CM000668.2:g.163765683T>G GRCh38
NC_000006.11:g.164186715T>G , CM000668.1:g.164186715T>G GRCh37
NC_000006.10:g.164106705T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001744452.1:n.410+6254T>G
XR_001744454.1:n.369+6295T>G
XR_001744455.1:n.346+6318T>G