Canonical Allele Identifier: CA2469660589
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2800463T= , CM000686.2:g.2800463T= GRCh38
NC_000024.9:g.2668504T= , CM000686.1:g.2668504T= GRCh37
NC_000024.8:g.2728504T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000679518.1:n.106+25724T=
ENST00000681787.1:n.106+25724T=
ENST00000681940.1:n.106+25724T=