Canonical Allele Identifier: CA2469660588
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2800443G= , CM000686.2:g.2800443G= GRCh38
NC_000024.9:g.2668484G= , CM000686.1:g.2668484G= GRCh37
NC_000024.8:g.2728484G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000679518.1:n.106+25704G=
ENST00000681787.1:n.106+25704G=
ENST00000681940.1:n.106+25704G=