Canonical Allele Identifier: CA6368969

Gene: IGSF9B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.133921088G>A , CM000673.2:g.133921088G>A	GRCh38
NC_000011.9:g.133790983G>A , CM000673.1:g.133790983G>A	GRCh37
NC_000011.8:g.133296193G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001277285.4:c.2637C>T MANE Select	NP_001264214.1:p.Phe879=
ENST00000533871.8:c.2637C>T MANE Select	ENSP00000436552.2:p.Phe879=
NM_001277285.1:c.2637C>T	NP_001264214.1:p.Phe879=
NM_001277285.2:c.2637C>T	NP_001264214.1:p.Phe879=
ENST00000321016.12:c.2637C>T	ENSP00000317980.8:p.Phe879=
ENST00000533871.6:c.2637C>T	ENSP00000436552.2:p.Phe879=
XM_006718795.2:c.1065C>T	XP_006718858.1:p.Phe355=
XM_006718795.3:c.1065C>T	XP_006718858.1:p.Phe355=
XM_011542691.1:c.2943C>T	XP_011540993.1:p.Phe981=
XM_011542691.3:c.2943C>T	XP_011540993.1:p.Phe981=
XM_011542692.1:c.2931C>T	XP_011540994.1:p.Phe977=
XM_011542692.3:c.2931C>T	XP_011540994.1:p.Phe977=
XM_011542693.1:c.2790C>T	XP_011540995.1:p.Phe930=
XM_011542694.1:c.2943C>T	XP_011540996.1:p.Phe981=
XM_011542694.3:c.2943C>T	XP_011540996.1:p.Phe981=
XM_011542695.1:c.2649C>T	XP_011540997.1:p.Phe883=
XM_011542695.2:c.2649C>T	XP_011540997.1:p.Phe883=
XM_017017393.1:c.2850C>T	XP_016872882.1:p.Phe950=
XM_017017394.2:c.2943C>T	XP_016872883.1:p.Phe981=
XM_017017395.2:c.2943C>T	XP_016872884.1:p.Phe981=
XM_017017396.1:c.1746C>T	XP_016872885.1:p.Phe582=
XM_024448402.1:c.2175C>T	XP_024304170.1:p.Phe725=
XR_947812.1:n.3176C>T
XR_947812.3:n.3380C>T