Canonical Allele Identifier: CA127232014
Gene:

Linked Data

dbSNP Id: rs532248450

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.126002795A>G , CM000667.2:g.126002795A>G GRCh38
NC_000005.9:g.125338488A>G , CM000667.1:g.125338488A>G GRCh37
NC_000005.8:g.125366387A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948737.1:n.565+3545T>C
XR_948738.1:n.497+5745T>C