Canonical Allele Identifier: CA469782219
Gene: RBP3 HGNC NCBI

Linked Data

dbSNP Id: rs1555211367
gnomAD v2: 10-48388970-C-T
gnomAD v4: 10-47350392-G-A
MyVariant Identifiers: chr10:g.48388970C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47350392G>A , CM000672.2:g.47350392G>A GRCh38
NC_000010.10:g.48388970C>T , CM000672.1:g.48388970C>T GRCh37
NC_000010.9:g.48008976C>T NCBI36
NG_029718.1:g.7022G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.1908G>A MANE Select ENSP00000463151.1:p.Leu636=
ENST00000584701.1:c.1908G>A ENSP00000463151.1:p.Leu636=
NM_002900.2:c.1908G>A NP_002891.1:p.Leu636=
NM_002900.3:c.1908G>A MANE Select NP_002891.1:p.Leu636=
Search 100 bp 5'
Search 100 bp 3'