Canonical Allele Identifier: CA1012755437
Gene:

Linked Data

dbSNP Id: rs1655908379

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.224068696T>G , CM000663.2:g.224068696T>G GRCh38
NC_000001.10:g.224256398T>G , CM000663.1:g.224256398T>G GRCh37
NC_000001.9:g.222323021T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949173.1:n.385+1042T>G
XR_001737824.1:n.242+1042T>G