Canonical Allele Identifier: CA1118643339
Gene:

Linked Data

dbSNP Id: rs1814948270

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.122395885C>T , CM000670.2:g.122395885C>T GRCh38
NC_000008.10:g.123408124C>T , CM000670.1:g.123408124C>T GRCh37
NC_000008.9:g.123477305C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928599.1:n.152+3287G>A
XR_928599.3:n.152+3287G>A