Canonical Allele Identifier: CA2469660111
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2791277G= , CM000686.2:g.2791277G= GRCh38
NC_000024.9:g.2659318G= , CM000686.1:g.2659318G= GRCh37
NC_000024.8:g.2719318G= NCBI36
NG_011751.1:g.1475C=

Transcript Alleles

HGVS Amino-acid change
ENST00000679518.1:n.106+16538G=
ENST00000681787.1:n.106+16538G=
ENST00000681940.1:n.106+16538G=