Canonical Allele Identifier: CA1392628888
Gene:

Linked Data

dbSNP Id: rs909737928

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.109743611A>T , CM000665.2:g.109743611A>T GRCh38
NC_000003.11:g.109462458A>T , CM000665.1:g.109462458A>T GRCh37
NC_000003.10:g.110945148A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924325.1:n.142+63416A>T