Canonical Allele Identifier: CA1350284060
Gene:

Linked Data

dbSNP Id: rs1575062670

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.21207165A>T , CM000665.2:g.21207165A>T GRCh38
NC_000003.11:g.21248657A>T , CM000665.1:g.21248657A>T GRCh37
NC_000003.10:g.21223661A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940646.1:n.254-3833A>T
XR_940646.2:n.547-3833A>T