Canonical Allele Identifier: CA2400653211

Gene: NF2

Linked Data

• dbSNP Id: rs2064699190

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29603623G>C , CM000684.2:g.29603623G>C	GRCh38
NC_000022.10:g.29999612G>C , CM000684.1:g.29999612G>C	GRCh37
NC_000022.9:g.28329612G>C	NCBI36
NG_009057.1:g.5068G>C , LRG_511:g.5068G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000672461.1:c.-376G>C	ENSP00000500919.1:n.-376G>C
ENST00000672805.1:c.-376G>C	ENSP00000500295.1:n.-376G>C
ENST00000338641.8:c.-376G>C	ENSP00000344666.4:n.-376G>C
ENST00000361452.8:c.-376G>C	ENSP00000354897.4:n.-376G>C
ENST00000403435.5:c.-376G>C	ENSP00000384029.1:n.-376G>C
ENST00000413209.6:c.-376G>C	ENSP00000409921.2:n.-376G>C
NM_000268.3:c.-376G>C , LRG_511t1:c.-376G>C	NP_000259.1:n.-376G>C
NM_016418.5:c.-376G>C , LRG_511t2:c.-376G>C	NP_057502.2:n.-376G>C
NM_181825.2:c.-376G>C	NP_861546.1:n.-376G>C
NM_181828.2:c.-376G>C	NP_861966.1:n.-376G>C
NM_181829.2:c.-376G>C	NP_861967.1:n.-376G>C
NM_181830.2:c.-376G>C	NP_861968.1:n.-376G>C
NM_181831.2:c.-376G>C	NP_861969.1:n.-376G>C
NM_181832.2:c.-376G>C	NP_861970.1:n.-376G>C
NM_181833.2:c.-376G>C	NP_861971.1:n.-376G>C
NR_156186.1:n.68G>C