Canonical Allele Identifier: CA388189569

Gene: RCBTB1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.49549530G>C , CM000675.2:g.49549530G>C	GRCh38
NC_000013.10:g.50123666G>C , CM000675.1:g.50123666G>C	GRCh37
NC_000013.9:g.49021667G>C	NCBI36
NG_046892.1:g.41077C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378302.7:c.973C>G MANE Select	ENSP00000367552.2:p.His325Asp
ENST00000258646.3:c.973C>G	ENSP00000258646.3:p.His325Asp
ENST00000378302.6:c.973C>G	ENSP00000367552.2:p.His325Asp
NM_018191.3:c.973C>G	NP_060661.3:p.His325Asp
XM_005266441.2:c.973C>G	XP_005266498.1:p.His325Asp
XM_011535133.1:c.973C>G	XP_011533435.1:p.His325Asp
XM_011535134.1:c.973C>G	XP_011533436.1:p.His325Asp
XM_011535135.1:c.586C>G	XP_011533437.1:p.His196Asp
XR_941613.1:n.1238C>G
NM_001352500.1:c.973C>G	NP_001339429.1:p.His325Asp
NM_001352501.1:c.973C>G	NP_001339430.1:p.His325Asp
NM_001352502.1:c.973C>G	NP_001339431.1:p.His325Asp
NM_001352503.1:c.973C>G	NP_001339432.1:p.His325Asp
NM_001352504.1:c.973C>G	NP_001339433.1:p.His325Asp
NM_001352505.1:c.973C>G	NP_001339434.1:p.His325Asp
NM_001352506.1:c.394C>G	NP_001339435.1:p.His132Asp
NR_148015.1:n.1392C>G
NR_148016.1:n.1348C>G
XM_011535135.2:c.586C>G	XP_011533437.1:p.His196Asp
XR_001749596.1:n.1238C>G
NM_018191.4:c.973C>G MANE Select	NP_060661.3:p.His325Asp
NM_001352500.2:c.973C>G	NP_001339429.1:p.His325Asp
NM_001352501.2:c.973C>G	NP_001339430.1:p.His325Asp
NM_001352502.2:c.973C>G	NP_001339431.1:p.His325Asp
NM_001352503.2:c.973C>G	NP_001339432.1:p.His325Asp
NM_001352505.2:c.973C>G	NP_001339434.1:p.His325Asp
NM_001352506.2:c.394C>G	NP_001339435.1:p.His132Asp
NR_148015.2:n.1367C>G
NR_148016.2:n.1323C>G
NM_001352504.2:c.973C>G	NP_001339433.1:p.His325Asp