Canonical Allele Identifier: CA1014650
Gene: RSBN1 HGNC NCBI

Linked Data

dbSNP Id: rs3789604

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.113812320T>G , CM000663.2:g.113812320T>G GRCh38
NC_000001.10:g.114354942T>G , CM000663.1:g.114354942T>G GRCh37
NC_000001.9:g.114156465T>G NCBI36
NG_011432.1:g.64434A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261441.9:c.93A>C MANE Select ENSP00000261441.5:p.Arg31=
ENST00000612242.4:c.93A>C ENSP00000479490.1:p.Arg31=
NM_018364.4:c.93A>C NP_060834.2:p.Arg31=
NR_130896.1:n.157A>C
XM_017001518.2:c.93A>C XP_016857007.1:p.Arg31=
NM_018364.5:c.93A>C MANE Select NP_060834.2:p.Arg31=
NR_130896.2:n.157A>C