Canonical Allele Identifier: CA2141801191
Gene:

Linked Data

dbSNP Id: rs1883745141

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.62501686T>G , CM000676.2:g.62501686T>G GRCh38
NC_000014.8:g.62968404T>G , CM000676.1:g.62968404T>G GRCh37
NC_000014.7:g.62038157T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943932.1:n.116-2355T>G
XR_943932.2:n.103-2355T>G