Canonical Allele Identifier: CA806430581
Gene:

Linked Data

dbSNP Id: rs1449147351

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159580829A>T , CM000667.2:g.159580829A>T GRCh38
NC_000005.9:g.159007837A>T , CM000667.1:g.159007837A>T GRCh37
NC_000005.8:g.158940415A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_941139.1:n.2075+394A>T
XR_941140.1:n.2075+394A>T
XR_941141.1:n.570+394A>T
XR_941139.2:n.2229+394A>T