Canonical Allele Identifier: CA1816081378
Gene:

Linked Data

dbSNP Id: rs1586448330

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.122396212G>A , CM000670.2:g.122396212G>A GRCh38
NC_000008.10:g.123408451G>A , CM000670.1:g.123408451G>A GRCh37
NC_000008.9:g.123477632G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928599.1:n.152+2960C>T
XR_928599.3:n.152+2960C>T