Canonical Allele Identifier: CA283656606
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs10500569

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.72722202G>T , CM000678.2:g.72722202G>T GRCh38
NC_000016.9:g.72756101G>T , CM000678.1:g.72756101G>T GRCh37
NC_000016.8:g.71313602G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017023920.1:n.581+8786G>T XP_016879409.1:p.=