Canonical Allele Identifier: CA1304775631
Gene: TTC21B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.165857487T= , CM000664.2:g.165857487T= GRCh38
NC_000002.11:g.166713997T= , CM000664.1:g.166713997T= GRCh37
NC_000002.10:g.166422243T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000392695.6:c.1563A=
ENST00000486672.5:n.733A=
ENST00000489714.5:n.635A=
NR_045375.2:n.1585A=