Canonical Allele Identifier: CA376672092
Gene: RBP3 HGNC NCBI

Linked Data

dbSNP Id: rs1555211413
gnomAD v2: 10-48388767-C-T
gnomAD v4: 10-47350595-G-A
MyVariant Identifiers: chr10:g.48388767C>T (hg19) chr10:g.47350595G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47350595G>A , CM000672.2:g.47350595G>A GRCh38
NC_000010.10:g.48388767C>T , CM000672.1:g.48388767C>T GRCh37
NC_000010.9:g.48008773C>T NCBI36
NG_029718.1:g.7225G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.2111G>A MANE Select ENSP00000463151.1:p.Ser704Asn
ENST00000584701.1:c.2111G>A ENSP00000463151.1:p.Ser704Asn
NM_002900.2:c.2111G>A NP_002891.1:p.Ser704Asn
NM_002900.3:c.2111G>A MANE Select NP_002891.1:p.Ser704Asn
Search 100 bp 5'
Search 100 bp 3'