Canonical Allele Identifier: CA376672156

Gene: RBP3

Linked Data

• dbSNP Id: rs1836954496
• gnomAD v3: 10-47350628-C-T
• gnomAD v4: 10-47350628-C-T
• MyVariant Identifiers: chr10:g.48388734G>A (hg19) ; chr10:g.47350628C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.47350628C>T , CM000672.2:g.47350628C>T	GRCh38
NC_000010.10:g.48388734G>A , CM000672.1:g.48388734G>A	GRCh37
NC_000010.9:g.48008740G>A	NCBI36
NG_029718.1:g.7258C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584701.2:c.2144C>T MANE Select	ENSP00000463151.1:p.Pro715Leu
ENST00000584701.1:c.2144C>T	ENSP00000463151.1:p.Pro715Leu
NM_002900.2:c.2144C>T	NP_002891.1:p.Pro715Leu
NM_002900.3:c.2144C>T MANE Select	NP_002891.1:p.Pro715Leu