Canonical Allele Identifier: CA755748311
Gene:

Linked Data

dbSNP Id: rs1256823533

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.118079695C>T , CM000664.2:g.118079695C>T GRCh38
NC_000002.11:g.118837271C>T , CM000664.1:g.118837271C>T GRCh37
NC_000002.10:g.118553741C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011512305.1:c.697-2163G>A XP_011510607.1:n.697-2163G>A
XR_001739662.2:n.138+8556G>A