Canonical Allele Identifier: CA397868518

Gene: TNFSF13 TNFSF12-TNFSF13

Linked Data

• dbSNP Id: rs11552708
• gnomAD v2: 17-7462555-G-C
• gnomAD v3: 17-7559238-G-C
• gnomAD v4: 17-7559238-G-C
• MyVariant Identifiers: chr17:g.7462555G>C (hg19) ; chr17:g.7559238G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7559238G>C , CM000679.2:g.7559238G>C	GRCh38
NC_000017.10:g.7462555G>C , CM000679.1:g.7462555G>C	GRCh37
NC_000017.9:g.7403279G>C	NCBI36
NG_029949.1:g.5947G>C
NG_052944.1:g.15181G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338784.9:c.199G>C (TNFSF13) MANE Select	ENSP00000343505.4:p.Gly67Arg
ENST00000293826.4:c.499-386G>C (TNFSF12-TNFSF13)	ENSP00000293826.4:n.499-386G>C
ENST00000338784.8:c.199G>C (TNFSF13)	ENSP00000343505.4:p.Gly67Arg
ENST00000349228.8:c.199G>C (TNFSF13)	ENSP00000314455.6:p.Gly67Arg
ENST00000380535.8:c.199G>C (TNFSF13)	ENSP00000369908.5:p.Gly67Arg
ENST00000396542.5:c.148G>C (TNFSF13)	ENSP00000379792.1:p.Gly50Arg
ENST00000396545.4:c.199G>C (TNFSF13)	ENSP00000379794.4:p.Gly67Arg
ENST00000436057.5:c.148G>C (TNFSF13)	ENSP00000410094.1:p.Gly50Arg
ENST00000438470.5:c.148G>C (TNFSF13)	ENSP00000390771.1:p.Gly50Arg
ENST00000483039.5:c.-71-608G>C (TNFSF13)	ENSP00000464998.1:n.-71-608G>C
ENST00000625791.2:c.199G>C (TNFSF13)	ENSP00000486052.1:p.Gly67Arg
NM_001198622.1:c.199G>C (TNFSF13)	NP_001185551.1:p.Gly67Arg
NM_001198623.1:c.199G>C (TNFSF13)	NP_001185552.1:p.Gly67Arg
NM_001198624.1:c.148G>C (TNFSF13)	NP_001185553.1:p.Gly50Arg
NM_003808.3:c.199G>C (TNFSF13)	NP_003799.1:p.Gly67Arg
NM_172087.2:c.199G>C (TNFSF13)	NP_742084.1:p.Gly67Arg
NM_172088.2:c.199G>C (TNFSF13)	NP_742085.1:p.Gly67Arg
NM_172089.3:c.499-386G>C (TNFSF12-TNFSF13)	NP_742086.1:n.499-386G>C
NR_073490.2:n.947G>C (TNFSF13)
NM_172089.4:c.499-386G>C (TNFSF12-TNFSF13)	NP_742086.1:n.499-386G>C
NM_001198622.2:c.199G>C (TNFSF13)	NP_001185551.1:p.Gly67Arg
NM_001198623.2:c.199G>C (TNFSF13)	NP_001185552.1:p.Gly67Arg
NM_001198624.2:c.148G>C (TNFSF13)	NP_001185553.1:p.Gly50Arg
NM_003808.4:c.199G>C (TNFSF13) MANE Select	NP_003799.1:p.Gly67Arg
NM_172087.3:c.199G>C (TNFSF13)	NP_742084.1:p.Gly67Arg
NM_172088.4:c.199G>C (TNFSF13)	NP_742085.1:p.Gly67Arg
NR_073490.3:n.489G>C (TNFSF13)