Canonical Allele Identifier: CA416364730

Gene: TNFRSF1B

Linked Data

• MyVariant Identifiers: chr1:g.12252962A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12192905A>C , CM000663.2:g.12192905A>C	GRCh38
NC_000001.10:g.12252962A>C , CM000663.1:g.12252962A>C	GRCh37
NC_000001.9:g.12175549A>C	NCBI36
NG_029791.1:g.30903A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000376259.7:c.594A>C MANE Select	ENSP00000365435.3:p.Ala198=
ENST00000376259.6:c.594A>C	ENSP00000365435.3:p.Ala198=
ENST00000489921.1:n.306A>C
ENST00000492361.1:n.583A>C
NM_001066.2:c.594A>C	NP_001057.1:p.Ala198=
XM_011542060.1:c.594A>C	XP_011540362.1:p.Ala198=
XM_011542061.1:c.594A>C	XP_011540363.1:p.Ala198=
XM_011542062.1:c.573A>C	XP_011540364.1:p.Ala191=
XM_011542063.1:c.594A>C	XP_011540365.1:p.Ala198=
XM_011542060.2:c.594A>C	XP_011540362.1:p.Ala198=
XM_011542063.2:c.594A>C	XP_011540365.1:p.Ala198=
XM_017002211.1:c.594A>C	XP_016857700.1:p.Ala198=
XM_017002214.1:c.9A>C	XP_016857703.1:p.Ala3=
XM_017002215.1:c.9A>C	XP_016857704.1:p.Ala3=
NM_001066.3:c.594A>C MANE Select	NP_001057.1:p.Ala198=