Canonical Allele Identifier: CA1304775642

Gene: TTC21B

Linked Data

• dbSNP Id: rs1662877977

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165857515T>G , CM000664.2:g.165857515T>G	GRCh38
NC_000002.11:g.166714025T>G , CM000664.1:g.166714025T>G	GRCh37
NC_000002.10:g.166422271T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000679356.1:c.*4248A>C	ENSP00000506245.1:n.*4248A>C
ENST00000679676.1:c.*4248A>C	ENSP00000505492.1:n.*4248A>C
ENST00000679931.1:c.*3583A>C	ENSP00000505632.1:n.*3583A>C
ENST00000679967.1:c.*4248A>C	ENSP00000506607.1:n.*4248A>C
ENST00000680249.1:n.3838A>C
ENST00000680327.1:c.*7241A>C	ENSP00000506639.1:n.*7241A>C
ENST00000680657.1:n.6442A>C
ENST00000680690.1:c.*7451A>C	ENSP00000506121.1:n.*7451A>C
ENST00000680888.1:c.*4248A>C	ENSP00000506276.1:n.*4248A>C
ENST00000680904.1:n.4703A>C
ENST00000680947.1:c.*7471A>C	ENSP00000506496.1:n.*7471A>C
ENST00000681024.1:c.*7989A>C	ENSP00000506449.1:n.*7989A>C
ENST00000681083.1:c.*7930A>C	ENSP00000506095.1:n.*7930A>C
ENST00000681167.1:n.8077A>C
ENST00000681483.1:c.*1351A>C	ENSP00000505499.1:n.*1351A>C
ENST00000681502.1:c.*11459A>C	ENSP00000505644.1:n.*11459A>C
ENST00000392695.6:c.1535A>C
ENST00000486672.5:n.705A>C
ENST00000489714.5:n.607A>C
NR_045375.2:n.1557A>C