Canonical Allele Identifier: CA1605795107
Gene:

Linked Data

dbSNP Id: rs1581337101

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1535904T>A , CM000668.2:g.1535904T>A GRCh38
NC_000006.11:g.1536139T>A , CM000668.1:g.1536139T>A GRCh37
NC_000006.10:g.1481138T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427861.2:n.234+16442A>T
XR_926380.1:n.218-2552T>A
XR_926381.1:n.1108-2552T>A
XR_926382.1:n.235-6725A>T
XR_926384.1:n.200-6725A>T
XR_001743921.1:n.235-6749A>T
XR_427861.3:n.234+16442A>T
XR_926381.2:n.1123-2552T>A