Canonical Allele Identifier: CA1580179066
Gene:

Linked Data

dbSNP Id: rs1749025244

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.126002812C>A , CM000667.2:g.126002812C>A GRCh38
NC_000005.9:g.125338505C>A , CM000667.1:g.125338505C>A GRCh37
NC_000005.8:g.125366404C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948737.1:n.565+3528G>T
XR_948738.1:n.497+5728G>T