Canonical Allele Identifier: CA1149396889
Gene:

Linked Data

dbSNP Id: rs1659179987

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2036389G>A , CM000663.2:g.2036389G>A GRCh38
NC_000001.10:g.1967828G>A , CM000663.1:g.1967828G>A GRCh37
NC_000001.9:g.1957688G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_946823.1:n.773+46C>T
XR_001737845.2:n.822C>T
XR_946823.3:n.776+46C>T