Canonical Allele Identifier: CA298296856
Gene:

Linked Data

dbSNP Id: rs903151417

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756640T>C , CM000680.2:g.31756640T>C GRCh38
NC_000018.9:g.29336603T>C , CM000680.1:g.29336603T>C GRCh37
NC_000018.8:g.27590601T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935338.1:n.66-5499T>C