Canonical Allele Identifier: CA1282459323
Gene:

Linked Data

dbSNP Id: rs1678097139

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.118086928A>G , CM000664.2:g.118086928A>G GRCh38
NC_000002.11:g.118844504A>G , CM000664.1:g.118844504A>G GRCh37
NC_000002.10:g.118560974A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011512305.1:c.696+1132T>C XP_011510607.1:n.696+1132T>C
XR_001739662.2:n.138+1323T>C