Canonical Allele Identifier: CA376672016
Gene: RBP3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.48388810G>A (hg19) chr10:g.47350552C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47350552C>T , CM000672.2:g.47350552C>T GRCh38
NC_000010.10:g.48388810G>A , CM000672.1:g.48388810G>A GRCh37
NC_000010.9:g.48008816G>A NCBI36
NG_029718.1:g.7182C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.2068C>T MANE Select ENSP00000463151.1:p.Leu690Phe
ENST00000584701.1:c.2068C>T ENSP00000463151.1:p.Leu690Phe
NM_002900.2:c.2068C>T NP_002891.1:p.Leu690Phe
NM_002900.3:c.2068C>T MANE Select NP_002891.1:p.Leu690Phe
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