Canonical Allele Identifier: CA1024936563

Gene: NF2

Linked Data

• dbSNP Id: rs2064699123
• gnomAD v3: 22-29603622-A-G
• gnomAD v4: 22-29603622-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29603622A>G , CM000684.2:g.29603622A>G	GRCh38
NC_000022.10:g.29999611A>G , CM000684.1:g.29999611A>G	GRCh37
NC_000022.9:g.28329611A>G	NCBI36
NG_009057.1:g.5067A>G , LRG_511:g.5067A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000672461.1:c.-377A>G	ENSP00000500919.1:n.-377A>G
ENST00000672805.1:c.-377A>G	ENSP00000500295.1:n.-377A>G
ENST00000338641.8:c.-377A>G	ENSP00000344666.4:n.-377A>G
ENST00000361452.8:c.-377A>G	ENSP00000354897.4:n.-377A>G
ENST00000403435.5:c.-377A>G	ENSP00000384029.1:n.-377A>G
ENST00000413209.6:c.-377A>G	ENSP00000409921.2:n.-377A>G
NM_000268.3:c.-377A>G , LRG_511t1:c.-377A>G	NP_000259.1:n.-377A>G
NM_016418.5:c.-377A>G , LRG_511t2:c.-377A>G	NP_057502.2:n.-377A>G
NM_181825.2:c.-377A>G	NP_861546.1:n.-377A>G
NM_181828.2:c.-377A>G	NP_861966.1:n.-377A>G
NM_181829.2:c.-377A>G	NP_861967.1:n.-377A>G
NM_181830.2:c.-377A>G	NP_861968.1:n.-377A>G
NM_181831.2:c.-377A>G	NP_861969.1:n.-377A>G
NM_181832.2:c.-377A>G	NP_861970.1:n.-377A>G
NM_181833.2:c.-377A>G	NP_861971.1:n.-377A>G
NR_156186.1:n.67A>G