Canonical Allele Identifier: CA297036489

Gene: RBBP8

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.22946205A>G , CM000680.2:g.22946205A>G	GRCh38
NC_000018.9:g.20526168A>G , CM000680.1:g.20526168A>G	GRCh37
NC_000018.8:g.18780166A>G	NCBI36
NG_012121.1:g.17874A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_002894.3:c.110-239A>G MANE Select	NP_002885.1:n.110-239A>G
ENST00000327155.10:c.110-239A>G MANE Select	ENSP00000323050.5:n.110-239A>G
NM_002894.2:c.110-239A>G	NP_002885.1:n.110-239A>G
NM_203291.1:c.110-239A>G	NP_976036.1:n.110-239A>G
NM_203291.2:c.110-239A>G	NP_976036.1:n.110-239A>G
NM_203292.1:c.110-239A>G	NP_976037.1:n.110-239A>G
NM_203292.2:c.110-239A>G	NP_976037.1:n.110-239A>G
ENST00000327155.9:c.110-239A>G	ENSP00000323050.5:n.110-239A>G
ENST00000360790.9:c.110-239A>G	ENSP00000354024.5:n.110-239A>G
ENST00000399721.6:c.110-239A>G	ENSP00000382627.2:n.110-239A>G
ENST00000399722.6:c.110-239A>G	ENSP00000382628.2:n.110-239A>G
ENST00000399725.6:c.110-239A>G	ENSP00000382630.2:n.110-239A>G
ENST00000579124.5:c.110-239A>G	ENSP00000462390.1:n.110-239A>G
ENST00000581819.5:c.110-239A>G	ENSP00000463439.1:n.110-239A>G
ENST00000582354.5:c.110-239A>G	ENSP00000463738.1:n.110-239A>G
XM_005258325.1:c.110-239A>G	XP_005258382.1:n.110-239A>G
XM_005258325.3:c.110-239A>G	XP_005258382.1:n.110-239A>G
XM_005258326.4:c.-807-239A>G	XP_005258383.1:n.-807-239A>G
XM_006722519.1:c.110-239A>G	XP_006722582.1:n.110-239A>G
XM_006722519.2:c.110-239A>G	XP_006722582.1:n.110-239A>G
XM_006722520.1:c.110-239A>G	XP_006722583.1:n.110-239A>G
XM_006722520.2:c.110-239A>G	XP_006722583.1:n.110-239A>G
XM_006722521.1:c.110-239A>G	XP_006722584.1:n.110-239A>G
XM_006722521.2:c.110-239A>G	XP_006722584.1:n.110-239A>G
XM_011526132.1:c.110-239A>G	XP_011524434.1:n.110-239A>G
XM_011526132.2:c.110-239A>G	XP_011524434.1:n.110-239A>G
XM_017025916.1:c.-873-239A>G	XP_016881405.1:n.-873-239A>G
XM_024451233.1:c.-251-239A>G	XP_024307001.1:n.-251-239A>G