Canonical Allele Identifier: CA9966673
Gene: RTEL1-TNFRSF6B HGNC NCBI
TNFRSF6B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63698573C>T , CM000682.2:g.63698573C>T GRCh38
NC_000020.10:g.62329926C>T , CM000682.1:g.62329926C>T GRCh37
NC_000020.9:g.61800370C>T NCBI36
NG_046961.1:g.6923C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000697815.1:n.3567C>T (RTEL1-TNFRSF6B)
ENST00000369996.3:c.*10C>T (TNFRSF6B) MANE Select ENSP00000359013.1:n.*10C>T
ENST00000496281.2:n.5736C>T (RTEL1-TNFRSF6B)
ENST00000369996.1:c.*10C>T (TNFRSF6B) ENSP00000359013.1:n.*10C>T
ENST00000480273.5:n.5640C>T (RTEL1-TNFRSF6B)
ENST00000482936.5:c.4820C>T (RTEL1-TNFRSF6B) ENSP00000457868.1:n.4820C>T
ENST00000492259.6:c.*2252C>T (RTEL1-TNFRSF6B) ENSP00000457428.1:n.*2252C>T
ENST00000496281.1:n.5207C>T (RTEL1-TNFRSF6B)
NM_003823.3:c.*10C>T (TNFRSF6B) NP_003814.1:n.*10C>T
NR_037882.1:n.5647C>T (RTEL1-TNFRSF6B)
NM_003823.4:c.*10C>T (TNFRSF6B) MANE Select NP_003814.1:n.*10C>T