Canonical Allele Identifier: CA760173593

Gene: TTC21B

Linked Data

• dbSNP Id: rs1488389971
• gnomAD v4: 2-165857513-AT-A
• MyVariant Identifiers: chr2:g.166714024del (hg19) ; chr2:g.165857514del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165857516del , CM000664.2:g.165857516del	GRCh38
NC_000002.11:g.166714026del , CM000664.1:g.166714026del	GRCh37
NC_000002.10:g.166422272del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000679356.1:c.*4249del	ENSP00000506245.1:n.*4249del
ENST00000679676.1:c.*4249del	ENSP00000505492.1:n.*4249del
ENST00000679931.1:c.*3584del	ENSP00000505632.1:n.*3584del
ENST00000679967.1:c.*4249del	ENSP00000506607.1:n.*4249del
ENST00000680249.1:n.3839del
ENST00000680327.1:c.*7242del	ENSP00000506639.1:n.*7242del
ENST00000680657.1:n.6443del
ENST00000680690.1:c.*7452del	ENSP00000506121.1:n.*7452del
ENST00000680888.1:c.*4249del	ENSP00000506276.1:n.*4249del
ENST00000680904.1:n.4704del
ENST00000680947.1:c.*7472del	ENSP00000506496.1:n.*7472del
ENST00000681024.1:c.*7990del	ENSP00000506449.1:n.*7990del
ENST00000681083.1:c.*7931del	ENSP00000506095.1:n.*7931del
ENST00000681167.1:n.8078del
ENST00000681483.1:c.*1352del	ENSP00000505499.1:n.*1352del
ENST00000681502.1:c.*11460del	ENSP00000505644.1:n.*11460del
ENST00000392695.6:c.1536del
ENST00000486672.5:n.706del
ENST00000489714.5:n.608del
NR_045375.2:n.1558del