Canonical Allele Identifier: CA2485976236
Gene:

Linked Data

dbSNP Id: rs1658288309

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.213682341C>T , CM000663.2:g.213682341C>T GRCh38
NC_000001.10:g.213855684C>T , CM000663.1:g.213855684C>T GRCh37
NC_000001.9:g.211922307C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001738463.1:n.601-49076C>T
XR_001738464.1:n.426-49076C>T