Canonical Allele Identifier: CA376671026
Gene: RBP3 HGNC NCBI

Linked Data

dbSNP Id: rs2132253993

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47350094T>C , CM000672.2:g.47350094T>C GRCh38
NC_000010.10:g.48389268A>G , CM000672.1:g.48389268A>G GRCh37
NC_000010.9:g.48009274A>G NCBI36
NG_029718.1:g.6724T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.1610T>C MANE Select ENSP00000463151.1:p.Val537Ala
ENST00000584701.1:c.1610T>C ENSP00000463151.1:p.Val537Ala
NM_002900.2:c.1610T>C NP_002891.1:p.Val537Ala
NM_002900.3:c.1610T>C MANE Select NP_002891.1:p.Val537Ala