Canonical Allele Identifier: CA1118643283
Gene:

Linked Data

dbSNP Id: rs1814945501

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.122395710G>A , CM000670.2:g.122395710G>A GRCh38
NC_000008.10:g.123407949G>A , CM000670.1:g.123407949G>A GRCh37
NC_000008.9:g.123477130G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928599.1:n.152+3462C>T
XR_928599.3:n.152+3462C>T