Canonical Allele Identifier: CA2065107431
Gene:

Linked Data

dbSNP Id: rs1876325050

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.115398750G>A , CM000674.2:g.115398750G>A GRCh38
NC_000012.11:g.115836555G>A , CM000674.1:g.115836555G>A GRCh37
NC_000012.10:g.114320938G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945389.1:n.697+8345C>T
XR_945389.2:n.701+8345C>T