Canonical Allele Identifier: CA498420292

Gene: TNFRSF13B

Linked Data

• MyVariant Identifiers: chr17:g.16852194T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948880T>C , CM000679.2:g.16948880T>C	GRCh38
NC_000017.10:g.16852194T>C , CM000679.1:g.16852194T>C	GRCh37
NC_000017.9:g.16792919T>C	NCBI36
NG_007281.1:g.28209A>G , LRG_120:g.28209A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261652.7:c.303A>G MANE Select	ENSP00000261652.2:p.Ala101=
ENST00000261652.6:c.303A>G	ENSP00000261652.2:p.Ala101=
ENST00000579315.5:c.303A>G	ENSP00000464069.1:p.Ala101=
ENST00000581616.2:n.306A>G
ENST00000582931.5:n.207A>G
ENST00000583789.1:c.165A>G	ENSP00000462952.1:p.Ala55=
ENST00000584950.5:c.165A>G	ENSP00000463582.1:p.Ala55=
NM_012452.2:c.303A>G , LRG_120t1:c.303A>G	NP_036584.1:p.Ala101=
NM_012452.3:c.303A>G MANE Select	NP_036584.1:p.Ala101=