Canonical Allele Identifier: CA2141801185
Gene:

Linked Data

dbSNP Id: rs1883745093

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.62501684G>T , CM000676.2:g.62501684G>T GRCh38
NC_000014.8:g.62968402G>T , CM000676.1:g.62968402G>T GRCh37
NC_000014.7:g.62038155G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943932.1:n.116-2357G>T
XR_943932.2:n.103-2357G>T