Canonical Allele Identifier: CA1304775624
Gene: TTC21B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.165857477T= , CM000664.2:g.165857477T= GRCh38
NC_000002.11:g.166713987T= , CM000664.1:g.166713987T= GRCh37
NC_000002.10:g.166422233T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000486672.5:n.743A=
ENST00000489714.5:n.645A=
NR_045375.2:n.1595A=