Canonical Allele Identifier: CA2710838319
Gene:

Linked Data

dbSNP Id: rs1761319404

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1535857A>T , CM000668.2:g.1535857A>T GRCh38
NC_000006.11:g.1536092A>T , CM000668.1:g.1536092A>T GRCh37
NC_000006.10:g.1481091A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427861.2:n.234+16489T>A
XR_926380.1:n.218-2599A>T
XR_926381.1:n.1108-2599A>T
XR_926382.1:n.235-6678T>A
XR_926384.1:n.200-6678T>A
XR_001743921.1:n.235-6702T>A
XR_427861.3:n.234+16489T>A
XR_926381.2:n.1123-2599A>T