Canonical Allele Identifier: CA376672149

Gene: RBP3

Linked Data

• dbSNP Id: rs1299574313
• gnomAD v3: 10-47350627-C-T
• gnomAD v4: 10-47350627-C-T
• MyVariant Identifiers: chr10:g.48388735G>A (hg19) ; chr10:g.47350627C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.47350627C>T , CM000672.2:g.47350627C>T	GRCh38
NC_000010.10:g.48388735G>A , CM000672.1:g.48388735G>A	GRCh37
NC_000010.9:g.48008741G>A	NCBI36
NG_029718.1:g.7257C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584701.2:c.2143C>T MANE Select	ENSP00000463151.1:p.Pro715Ser
ENST00000584701.1:c.2143C>T	ENSP00000463151.1:p.Pro715Ser
NM_002900.2:c.2143C>T	NP_002891.1:p.Pro715Ser
NM_002900.3:c.2143C>T MANE Select	NP_002891.1:p.Pro715Ser