Canonical Allele Identifier: CA1118643301
Gene:

Linked Data

dbSNP Id: rs1814946621

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.122395774G>T , CM000670.2:g.122395774G>T GRCh38
NC_000008.10:g.123408013G>T , CM000670.1:g.123408013G>T GRCh37
NC_000008.9:g.123477194G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928599.1:n.152+3398C>A
XR_928599.3:n.152+3398C>A