Canonical Allele Identifier: CA752278152

Gene: NF2

Linked Data

• dbSNP Id: rs1486120767
• MyVariant Identifiers: chr22:g.29999574A>G (hg19) ; chr22:g.29603585A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29603585A>G , CM000684.2:g.29603585A>G	GRCh38
NC_000022.10:g.29999574A>G , CM000684.1:g.29999574A>G	GRCh37
NC_000022.9:g.28329574A>G	NCBI36
NG_009057.1:g.5030A>G , LRG_511:g.5030A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000672805.1:c.-414A>G	ENSP00000500295.1:n.-414A>G
ENST00000338641.8:c.-414A>G	ENSP00000344666.4:n.-414A>G
ENST00000413209.6:c.-414A>G	ENSP00000409921.2:n.-414A>G
NM_000268.3:c.-414A>G , LRG_511t1:c.-414A>G	NP_000259.1:n.-414A>G
NM_016418.5:c.-414A>G , LRG_511t2:c.-414A>G	NP_057502.2:n.-414A>G
NM_181825.2:c.-414A>G	NP_861546.1:n.-414A>G
NM_181828.2:c.-414A>G	NP_861966.1:n.-414A>G
NM_181829.2:c.-414A>G	NP_861967.1:n.-414A>G
NM_181830.2:c.-414A>G	NP_861968.1:n.-414A>G
NM_181831.2:c.-414A>G	NP_861969.1:n.-414A>G
NM_181832.2:c.-414A>G	NP_861970.1:n.-414A>G
NM_181833.2:c.-414A>G	NP_861971.1:n.-414A>G
NR_156186.1:n.30A>G