Canonical Allele Identifier: CA2400653250

Gene: NF2

Linked Data

• dbSNP Id: rs2064701441
• gnomAD v4: 22-29603693-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29603693C>G , CM000684.2:g.29603693C>G	GRCh38
NC_000022.10:g.29999682C>G , CM000684.1:g.29999682C>G	GRCh37
NC_000022.9:g.28329682C>G	NCBI36
NG_009057.1:g.5138C>G , LRG_511:g.5138C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000361166.10:c.-306C>G	ENSP00000354529.6:n.-306C>G
ENST00000673312.2:c.-306C>G	ENSP00000500186.2:n.-306C>G
ENST00000338641.10:c.-306C>G MANE Select	ENSP00000344666.5:n.-306C>G
ENST00000672461.1:c.-306C>G	ENSP00000500919.1:n.-306C>G
ENST00000672805.1:c.-306C>G	ENSP00000500295.1:n.-306C>G
ENST00000672896.1:c.-306C>G	ENSP00000500117.1:n.-306C>G
ENST00000338641.8:c.-306C>G	ENSP00000344666.4:n.-306C>G
ENST00000361452.8:c.-306C>G	ENSP00000354897.4:n.-306C>G
ENST00000403435.5:c.-306C>G	ENSP00000384029.1:n.-306C>G
ENST00000403999.7:c.-306C>G	ENSP00000384797.3:n.-306C>G
ENST00000413209.6:c.-306C>G	ENSP00000409921.2:n.-306C>G
NM_000268.3:c.-306C>G , LRG_511t1:c.-306C>G	NP_000259.1:n.-306C>G
NM_016418.5:c.-306C>G , LRG_511t2:c.-306C>G	NP_057502.2:n.-306C>G
NM_181825.2:c.-306C>G	NP_861546.1:n.-306C>G
NM_181828.2:c.-306C>G	NP_861966.1:n.-306C>G
NM_181829.2:c.-306C>G	NP_861967.1:n.-306C>G
NM_181830.2:c.-306C>G	NP_861968.1:n.-306C>G
NM_181831.2:c.-306C>G	NP_861969.1:n.-306C>G
NM_181832.2:c.-306C>G	NP_861970.1:n.-306C>G
NM_181833.2:c.-306C>G	NP_861971.1:n.-306C>G
NR_156186.1:n.138C>G
NM_000268.4:c.-306C>G MANE Select	NP_000259.1:n.-306C>G
NM_181825.3:c.-306C>G	NP_861546.1:n.-306C>G
NM_181828.3:c.-306C>G	NP_861966.1:n.-306C>G
NM_181829.3:c.-306C>G	NP_861967.1:n.-306C>G
NM_181830.3:c.-306C>G	NP_861968.1:n.-306C>G
NM_181831.3:c.-306C>G	NP_861969.1:n.-306C>G
NM_181832.3:c.-306C>G	NP_861970.1:n.-306C>G
NR_156186.2:n.61C>G
NM_181833.3:c.-306C>G	NP_861971.1:n.-306C>G