Canonical Allele Identifier: CA9966408

Gene: RTEL1-TNFRSF6B TNFRSF6B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63697085C>T , CM000682.2:g.63697085C>T	GRCh38
NC_000020.10:g.62328438C>T , CM000682.1:g.62328438C>T	GRCh37
NC_000020.9:g.61798882C>T	NCBI36
NG_033901.1:g.44276C>T
NG_046961.1:g.5435C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_003823.4:c.318C>T (TNFRSF6B) MANE Select	NP_003814.1:p.His106=
ENST00000369996.3:c.318C>T (TNFRSF6B) MANE Select	ENSP00000359013.1:p.His106=
NM_003823.3:c.318C>T (TNFRSF6B)	NP_003814.1:p.His106=
NR_037882.1:n.5052C>T (RTEL1-TNFRSF6B)
ENST00000369996.1:c.318C>T (TNFRSF6B)	ENSP00000359013.1:p.His106=
ENST00000480273.5:n.5045C>T (RTEL1-TNFRSF6B)
ENST00000482936.5:c.4225C>T (RTEL1-TNFRSF6B)	ENSP00000457868.1:n.4225C>T
ENST00000492259.6:c.*1657C>T (RTEL1-TNFRSF6B)	ENSP00000457428.1:n.*1657C>T
ENST00000496281.1:n.4612C>T (RTEL1-TNFRSF6B)
ENST00000496281.2:n.5141C>T (RTEL1-TNFRSF6B)
ENST00000697815.1:n.2972C>T (RTEL1-TNFRSF6B)