Canonical Allele Identifier: CA10262524
Gene: TNFRSF13C HGNC NCBI

Linked Data

ClinVar Variation Id: 341883
ClinVar RCV Id: RCV000648324 RCV001643043
dbSNP Id: rs77874543
ExAC: 22:42322716 G / C
gnomAD v2: 22-42322716-G-C
gnomAD v3: 22-41926712-G-C
gnomAD v4: 22-41926712-G-C
MyVariant Identifiers: chr22:g.42322716G>C (hg19) chr22:g.41926712G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.41926712G>C , CM000684.2:g.41926712G>C GRCh38
NC_000022.10:g.42322716G>C , CM000684.1:g.42322716G>C GRCh37
NC_000022.9:g.40652662G>C NCBI36
NG_007579.1:g.5106C>G , LRG_184:g.5106C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000291232.5:c.62C>G MANE Select ENSP00000291232.3:p.Pro21Arg
ENST00000291232.4:c.62C>G ENSP00000291232.3:p.Pro21Arg
NM_052945.3:c.62C>G , LRG_184t1:c.62C>G NP_443177.1:p.Pro21Arg
NM_052945.4:c.62C>G MANE Select NP_443177.1:p.Pro21Arg
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