Canonical Allele Identifier: CA1649534288
Gene:

Linked Data

dbSNP Id: rs1773162578

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98102526T>C , CM000668.2:g.98102526T>C GRCh38
NC_000006.11:g.98550402T>C , CM000668.1:g.98550402T>C GRCh37
NC_000006.10:g.98657123T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.456+3256T>C
XR_942809.1:n.456+3256T>C