Canonical Allele Identifier: CA2523830249
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2800278C>A , CM000686.2:g.2800278C>A GRCh38
NC_000024.9:g.2668319C>A , CM000686.1:g.2668319C>A GRCh37
NC_000024.8:g.2728319C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000679518.1:n.106+25539C>A
ENST00000681787.1:n.106+25539C>A
ENST00000681940.1:n.106+25539C>A