Canonical Allele Identifier: CA1304775645

Gene: TTC21B

Linked Data

• dbSNP Id: rs1684316835

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165857522G>C , CM000664.2:g.165857522G>C	GRCh38
NC_000002.11:g.166714032G>C , CM000664.1:g.166714032G>C	GRCh37
NC_000002.10:g.166422278G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000679356.1:c.*4241C>G	ENSP00000506245.1:n.*4241C>G
ENST00000679676.1:c.*4241C>G	ENSP00000505492.1:n.*4241C>G
ENST00000679931.1:c.*3576C>G	ENSP00000505632.1:n.*3576C>G
ENST00000679967.1:c.*4241C>G	ENSP00000506607.1:n.*4241C>G
ENST00000680249.1:n.3831C>G
ENST00000680327.1:c.*7234C>G	ENSP00000506639.1:n.*7234C>G
ENST00000680657.1:n.6435C>G
ENST00000680690.1:c.*7444C>G	ENSP00000506121.1:n.*7444C>G
ENST00000680888.1:c.*4241C>G	ENSP00000506276.1:n.*4241C>G
ENST00000680904.1:n.4696C>G
ENST00000680947.1:c.*7464C>G	ENSP00000506496.1:n.*7464C>G
ENST00000681024.1:c.*7982C>G	ENSP00000506449.1:n.*7982C>G
ENST00000681083.1:c.*7923C>G	ENSP00000506095.1:n.*7923C>G
ENST00000681167.1:n.8070C>G
ENST00000681483.1:c.*1344C>G	ENSP00000505499.1:n.*1344C>G
ENST00000681502.1:c.*11452C>G	ENSP00000505644.1:n.*11452C>G
ENST00000681952.1:c.*583C>G	ENSP00000506400.1:n.*583C>G
ENST00000392695.6:c.1528C>G
ENST00000486672.5:n.698C>G
ENST00000489714.5:n.600C>G
NR_045375.2:n.1550C>G