Canonical Allele Identifier: CA1816081430
Gene:

Linked Data

dbSNP Id: rs1814953635

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.122396333T>A , CM000670.2:g.122396333T>A GRCh38
NC_000008.10:g.123408572T>A , CM000670.1:g.123408572T>A GRCh37
NC_000008.9:g.123477753T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928599.1:n.152+2839A>T
XR_928599.3:n.152+2839A>T