Canonical Allele Identifier: CA537131635

Gene: TTC21B

Linked Data

• dbSNP Id: rs1050388890
• gnomAD v2: 2-166713997-T-A
• gnomAD v3: 2-165857487-T-A
• gnomAD v4: 2-165857487-T-A
• MyVariant Identifiers: chr2:g.166713997T>A (hg19) ; chr2:g.165857487T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165857487T>A , CM000664.2:g.165857487T>A	GRCh38
NC_000002.11:g.166713997T>A , CM000664.1:g.166713997T>A	GRCh37
NC_000002.10:g.166422243T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392695.6:c.1563A>T
ENST00000486672.5:n.733A>T
ENST00000489714.5:n.635A>T
NR_045375.2:n.1585A>T