Canonical Allele Identifier: CA298296855
Gene:

Linked Data

dbSNP Id: rs542228429

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756637C>T , CM000680.2:g.31756637C>T GRCh38
NC_000018.9:g.29336600C>T , CM000680.1:g.29336600C>T GRCh37
NC_000018.8:g.27590598C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935338.1:n.66-5502C>T