Canonical Allele Identifier: CA262352021
Gene:

Linked Data

dbSNP Id: rs959480254

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.62501741A>G , CM000676.2:g.62501741A>G GRCh38
NC_000014.8:g.62968459A>G , CM000676.1:g.62968459A>G GRCh37
NC_000014.7:g.62038212A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943932.1:n.116-2300A>G
XR_943932.2:n.103-2300A>G