Canonical Allele Identifier: CA2206404287
Gene:

Linked Data

dbSNP Id: rs1450809794

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9249719A>C , CM000678.2:g.9249719A>C GRCh38
NC_000016.9:g.9343576A>C , CM000678.1:g.9343576A>C GRCh37
NC_000016.8:g.9251077A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933054.1:n.70+64986A>C