Canonical Allele Identifier: CA1591798734
Gene:

Linked Data

dbSNP Id: rs1760955067

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.152354606G>A , CM000667.2:g.152354606G>A GRCh38
NC_000005.9:g.151734167G>A , CM000667.1:g.151734167G>A GRCh37
NC_000005.8:g.151714360G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_944433.1:n.196+16743G>A
XR_944433.2:n.197+16743G>A