Canonical Allele Identifier: CA15834210

Gene: CORO2B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68600650C>T , CM000677.2:g.68600650C>T	GRCh38
NC_000015.9:g.68892989C>T , CM000677.1:g.68892989C>T	GRCh37
NC_000015.8:g.66680043C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261861.10:c.15+21373C>T MANE Select	ENSP00000261861.6:n.15+21373C>T
ENST00000261861.9:c.-1+21373C>T	ENSP00000261861.5:n.-1+21373C>T
ENST00000566799.5:c.15+21373C>T	ENSP00000454783.1:n.15+21373C>T
NM_006091.4:c.15+21373C>T	NP_006082.3:n.15+21373C>T
XM_005254124.1:c.3+41037C>T	XP_005254181.1:n.3+41037C>T
XM_011521159.1:c.-1+20000C>T	XP_011519461.1:n.-1+20000C>T
NM_001324014.1:c.1-44510C>T	NP_001310943.1:n.1-44510C>T
NM_006091.5:c.15+21373C>T MANE Select	NP_006082.3:n.15+21373C>T