Canonical Allele Identifier: CA1282456522
Gene:

Linked Data

dbSNP Id: rs1678010049

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.118079853T>C , CM000664.2:g.118079853T>C GRCh38
NC_000002.11:g.118837429T>C , CM000664.1:g.118837429T>C GRCh37
NC_000002.10:g.118553899T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011512305.1:c.697-2321A>G XP_011510607.1:n.697-2321A>G
XR_001739662.2:n.138+8398A>G