Canonical Allele Identifier: CA2284269333
Gene:

Linked Data

dbSNP Id: rs1969409210

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10382910G>T , CM000680.2:g.10382910G>T GRCh38
NC_000018.9:g.10382907G>T , CM000680.1:g.10382907G>T GRCh37
NC_000018.8:g.10372907G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935143.1:n.919+1557G>T