Canonical Allele Identifier: CA1149396847
Gene:

Linked Data

dbSNP Id: rs1659179060

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2036355C>G , CM000663.2:g.2036355C>G GRCh38
NC_000001.10:g.1967794C>G , CM000663.1:g.1967794C>G GRCh37
NC_000001.9:g.1957654C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_946823.1:n.773+80G>C
XR_001737845.2:n.856G>C
XR_946823.3:n.776+80G>C