Canonical Allele Identifier: CA2509815094
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2791289T>A , CM000686.2:g.2791289T>A GRCh38
NC_000024.9:g.2659330T>A , CM000686.1:g.2659330T>A GRCh37
NC_000024.8:g.2719330T>A NCBI36
NG_011751.1:g.1463A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000679518.1:n.106+16550T>A
ENST00000681787.1:n.106+16550T>A
ENST00000681940.1:n.106+16550T>A