Canonical Allele Identifier: CA2581058098

Gene: IGSF9B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.133930324C>T , CM000673.2:g.133930324C>T	GRCh38
NC_000011.9:g.133800219C>T , CM000673.1:g.133800219C>T	GRCh37
NC_000011.8:g.133305429C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000533871.8:c.1520-542G>A MANE Select	ENSP00000436552.2:n.1520-542G>A
ENST00000321016.12:c.1520-542G>A	ENSP00000317980.8:n.1520-542G>A
ENST00000527648.2:n.1250-542G>A
ENST00000533871.6:c.1520-542G>A	ENSP00000436552.2:n.1520-542G>A
NM_001277285.1:c.1520-542G>A	NP_001264214.1:n.1520-542G>A
XM_006718795.2:c.59+660G>A	XP_006718858.1:n.59+660G>A
XM_011542691.1:c.1814-542G>A	XP_011540993.1:n.1814-542G>A
XM_011542692.1:c.1814-542G>A	XP_011540994.1:n.1814-542G>A
XM_011542693.1:c.1661-542G>A	XP_011540995.1:n.1661-542G>A
XM_011542694.1:c.1814-542G>A	XP_011540996.1:n.1814-542G>A
XM_011542695.1:c.1520-542G>A	XP_011540997.1:n.1520-542G>A
XR_947812.1:n.2047-542G>A
XM_006718795.3:c.59+660G>A	XP_006718858.1:n.59+660G>A
XM_011542691.3:c.1814-542G>A	XP_011540993.1:n.1814-542G>A
XM_011542692.3:c.1814-542G>A	XP_011540994.1:n.1814-542G>A
XM_011542694.3:c.1814-542G>A	XP_011540996.1:n.1814-542G>A
XM_011542695.2:c.1520-542G>A	XP_011540997.1:n.1520-542G>A
XM_017017393.1:c.1721-542G>A	XP_016872882.1:n.1721-542G>A
XM_017017394.2:c.1814-542G>A	XP_016872883.1:n.1814-542G>A
XM_017017395.2:c.1814-542G>A	XP_016872884.1:n.1814-542G>A
XM_017017396.1:c.617-542G>A	XP_016872885.1:n.617-542G>A
XM_024448402.1:c.1046-542G>A	XP_024304170.1:n.1046-542G>A
XR_947812.3:n.2251-542G>A
NM_001277285.2:c.1520-542G>A	NP_001264214.1:n.1520-542G>A
NM_001277285.4:c.1520-542G>A MANE Select	NP_001264214.1:n.1520-542G>A