Canonical Allele Identifier: CA376670025

Gene: RBP3

Linked Data

• dbSNP Id: rs1555211224
• gnomAD v2: 10-48389386-C-T
• gnomAD v4: 10-47349976-G-A
• MyVariant Identifiers: chr10:g.48389386C>T (hg19) ; chr10:g.47349976G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.47349976G>A , CM000672.2:g.47349976G>A	GRCh38
NC_000010.10:g.48389386C>T , CM000672.1:g.48389386C>T	GRCh37
NC_000010.9:g.48009392C>T	NCBI36
NG_029718.1:g.6606G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584701.2:c.1492G>A MANE Select	ENSP00000463151.1:p.Gly498Ser
ENST00000584701.1:c.1492G>A	ENSP00000463151.1:p.Gly498Ser
NM_002900.2:c.1492G>A	NP_002891.1:p.Gly498Ser
NM_002900.3:c.1492G>A MANE Select	NP_002891.1:p.Gly498Ser