Canonical Allele Identifier: CA16841575
Gene:

Linked Data

dbSNP Id: rs554579860

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2036348G>C , CM000663.2:g.2036348G>C GRCh38
NC_000001.10:g.1967787G>C , CM000663.1:g.1967787G>C GRCh37
NC_000001.9:g.1957647G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_946823.1:n.773+87C>G
XR_001737845.2:n.863C>G
XR_946823.3:n.776+87C>G