Canonical Allele Identifier: CA1149396850
Gene:

Linked Data

dbSNP Id: rs1557452657

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2036358G>A , CM000663.2:g.2036358G>A GRCh38
NC_000001.10:g.1967797G>A , CM000663.1:g.1967797G>A GRCh37
NC_000001.9:g.1957657G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_946823.1:n.773+77C>T
XR_001737845.2:n.853C>T
XR_946823.3:n.776+77C>T