Canonical Allele Identifier: CA2547829410
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2791297A>T , CM000686.2:g.2791297A>T GRCh38
NC_000024.9:g.2659338A>T , CM000686.1:g.2659338A>T GRCh37
NC_000024.8:g.2719338A>T NCBI36
NG_011751.1:g.1455T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000679518.1:n.106+16558A>T
ENST00000681787.1:n.106+16558A>T
ENST00000681940.1:n.106+16558A>T