Canonical Allele Identifier: CA1282459285
Gene:

Linked Data

dbSNP Id: rs1678095858

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.118086834A>T , CM000664.2:g.118086834A>T GRCh38
NC_000002.11:g.118844410A>T , CM000664.1:g.118844410A>T GRCh37
NC_000002.10:g.118560880A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011512305.1:c.696+1226T>A XP_011510607.1:n.696+1226T>A
XR_001739662.2:n.138+1417T>A