Canonical Allele Identifier: CA376671933
Gene: RBP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 845988
ClinVar RCV Id: RCV001049175
dbSNP Id: rs1192156226
gnomAD v2: 10-48388855-T-C
gnomAD v3: 10-47350507-A-G
gnomAD v4: 10-47350507-A-G
MyVariant Identifiers: chr10:g.48388855T>C (hg19) chr10:g.47350507A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47350507A>G , CM000672.2:g.47350507A>G GRCh38
NC_000010.10:g.48388855T>C , CM000672.1:g.48388855T>C GRCh37
NC_000010.9:g.48008861T>C NCBI36
NG_029718.1:g.7137A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.2023A>G MANE Select ENSP00000463151.1:p.Thr675Ala
ENST00000584701.1:c.2023A>G ENSP00000463151.1:p.Thr675Ala
NM_002900.2:c.2023A>G NP_002891.1:p.Thr675Ala
NM_002900.3:c.2023A>G MANE Select NP_002891.1:p.Thr675Ala
Search 100 bp 5'
Search 100 bp 3'