Canonical Allele Identifier: CA4674939

Gene: TNFRSF10A

Linked Data

• dbSNP Id: rs773295396
• ExAC: 8:23069616 T / G
• gnomAD v2: 8-23069616-T-G
• gnomAD v3: 8-23212103-T-G
• gnomAD v4: 8-23212103-T-G
• MyVariant Identifiers: chr8:g.23069616T>G (hg19) ; chr8:g.23212103T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23212103T>G , CM000670.2:g.23212103T>G	GRCh38
NC_000008.10:g.23069616T>G , CM000670.1:g.23069616T>G	GRCh37
NC_000008.9:g.23125561T>G	NCBI36
NG_032107.1:g.18065A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221132.8:c.403+13A>C MANE Select	ENSP00000221132.3:n.403+13A>C
ENST00000221132.7:c.403+13A>C	ENSP00000221132.3:n.403+13A>C
ENST00000524158.5:c.-204+13A>C	ENSP00000428884.1:n.-204+13A>C
ENST00000613472.1:c.32-9444A>C	ENSP00000480778.1:n.32-9444A>C
NM_003844.3:c.403+13A>C	NP_003835.3:n.403+13A>C
NM_003844.4:c.403+13A>C MANE Select	NP_003835.3:n.403+13A>C