Canonical Allele Identifier: CA2302316771
Gene:

Linked Data

dbSNP Id: rs2021992783

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.49645830T>C , CM000680.2:g.49645830T>C GRCh38
NC_000018.9:g.47172200T>C , CM000680.1:g.47172200T>C GRCh37
NC_000018.8:g.45426198T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935461.1:n.162-16204T>C
XR_001753446.1:n.898-16204T>C