Canonical Allele Identifier: CA498420176

Gene: TNFRSF13B

Linked Data

• MyVariant Identifiers: chr17:g.16852110A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948796A>G , CM000679.2:g.16948796A>G	GRCh38
NC_000017.10:g.16852110A>G , CM000679.1:g.16852110A>G	GRCh37
NC_000017.9:g.16792835A>G	NCBI36
NG_007281.1:g.28293T>C , LRG_120:g.28293T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.387T>C MANE Select	ENSP00000261652.2:p.Asn129=
ENST00000261652.6:c.387T>C	ENSP00000261652.2:p.Asn129=
ENST00000579315.5:c.387T>C	ENSP00000464069.1:p.Asn129=
ENST00000581616.2:n.390T>C
ENST00000582931.5:n.291T>C
ENST00000583789.1:c.249T>C	ENSP00000462952.1:p.Asn83=
ENST00000584950.5:c.249T>C	ENSP00000463582.1:p.Asn83=
NM_012452.2:c.387T>C , LRG_120t1:c.387T>C	NP_036584.1:p.Asn129=
NM_012452.3:c.387T>C MANE Select	NP_036584.1:p.Asn129=