Canonical Allele Identifier: CA1816081235
Gene:

Linked Data

dbSNP Id: rs1814948451

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.122395897T>A , CM000670.2:g.122395897T>A GRCh38
NC_000008.10:g.123408136T>A , CM000670.1:g.123408136T>A GRCh37
NC_000008.9:g.123477317T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928599.1:n.152+3275A>T
XR_928599.3:n.152+3275A>T