Canonical Allele Identifier: CA773444789
Gene:

Linked Data

dbSNP Id: rs1340937371

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.57788881A>C , CM000679.2:g.57788881A>C GRCh38
NC_000017.10:g.55866242A>C , CM000679.1:g.55866242A>C GRCh37
NC_000017.9:g.53221241A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_934881.1:n.1608-16685T>G
XR_934881.3:n.3815-16685T>G