Canonical Allele Identifier: CA1580179053
Gene:

Linked Data

dbSNP Id: rs1749024967

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.126002785G>A , CM000667.2:g.126002785G>A GRCh38
NC_000005.9:g.125338478G>A , CM000667.1:g.125338478G>A GRCh37
NC_000005.8:g.125366377G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948737.1:n.565+3555C>T
XR_948738.1:n.497+5755C>T