Canonical Allele Identifier: CA1304775626
Gene: TTC21B HGNC NCBI

Linked Data

dbSNP Id: rs1684316090

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.165857478A>G , CM000664.2:g.165857478A>G GRCh38
NC_000002.11:g.166713988A>G , CM000664.1:g.166713988A>G GRCh37
NC_000002.10:g.166422234A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000392695.6:c.1572T>C
ENST00000486672.5:n.742T>C
ENST00000489714.5:n.644T>C
NR_045375.2:n.1594T>C