Canonical Allele Identifier: CA2695244490
Gene:

Linked Data

dbSNP Id: rs554579860

Genomic Alleles

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

Transcript Alleles

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