Canonical Allele Identifier: CA987758026
Gene:

Linked Data

dbSNP Id: rs1969408402

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10382823T>C , CM000680.2:g.10382823T>C GRCh38
NC_000018.9:g.10382820T>C , CM000680.1:g.10382820T>C GRCh37
NC_000018.8:g.10372820T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935143.1:n.919+1470T>C