Canonical Allele Identifier: CA2509421413
Gene:

Linked Data

dbSNP Id: rs2127969087

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98014496G>T , CM000668.2:g.98014496G>T GRCh38
NC_000006.11:g.98462372G>T , CM000668.1:g.98462372G>T GRCh37
NC_000006.10:g.98569093G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.371+45030G>T
XR_942809.1:n.371+45030G>T