Canonical Allele Identifier: CA1769199451
Gene:

Linked Data

dbSNP Id: rs2071239801

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.20130132T>C , CM000670.2:g.20130132T>C GRCh38
NC_000008.10:g.19987643T>C , CM000670.1:g.19987643T>C GRCh37
NC_000008.9:g.20031923T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949563.1:n.3408+213T>C
XR_949563.2:n.3400+213T>C