Canonical Allele Identifier: CA14680570

Gene: SBNO2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1124836A>G , CM000681.2:g.1124836A>G	GRCh38
NC_000019.9:g.1124835A>G , CM000681.1:g.1124835A>G	GRCh37
NC_000019.8:g.1075835A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361757.8:c.442-814T>C MANE Select	ENSP00000354733.2:n.442-814T>C
ENST00000361757.7:c.442-814T>C	ENSP00000354733.2:n.442-814T>C
ENST00000438103.6:c.271-814T>C	ENSP00000400762.1:n.271-814T>C
ENST00000587024.5:c.442-814T>C	ENSP00000468520.1:n.442-814T>C
ENST00000592222.5:n.295-814T>C
NM_001100122.1:c.271-814T>C	NP_001093592.1:n.271-814T>C
NM_014963.2:c.442-814T>C	NP_055778.2:n.442-814T>C
XM_005259519.3:c.442-814T>C	XP_005259576.1:n.442-814T>C
XM_005259520.2:c.442-814T>C	XP_005259577.1:n.442-814T>C
XM_011527803.1:c.220-814T>C	XP_011526105.1:n.220-814T>C
XM_011527804.1:c.442-814T>C	XP_011526106.1:n.442-814T>C
XM_011527804.3:c.442-814T>C	XP_011526106.1:n.442-814T>C
NM_014963.3:c.442-814T>C MANE Select	NP_055778.2:n.442-814T>C
NM_001100122.2:c.271-814T>C	NP_001093592.1:n.271-814T>C