Canonical Allele Identifier: CA364068239

Gene: NCR2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.41350690G>C , CM000668.2:g.41350690G>C	GRCh38
NC_000006.11:g.41318428G>C , CM000668.1:g.41318428G>C	GRCh37
NC_000006.10:g.41426406G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_004828.4:c.657G>C MANE Select	NP_004819.2:p.Trp219Cys
ENST00000373089.10:c.657G>C MANE Select	ENSP00000362181.5:p.Trp219Cys
NM_001199509.1:c.800G>C	NP_001186438.1:p.Gly267Ala
NM_001199509.2:c.800G>C	NP_001186438.1:p.Gly267Ala
NM_001199510.1:c.764G>C	NP_001186439.1:p.Gly255Ala
NM_001199510.2:c.764G>C	NP_001186439.1:p.Gly255Ala
NM_004828.3:c.657G>C	NP_004819.2:p.Trp219Cys
ENST00000373083.8:c.764G>C	ENSP00000362175.4:p.Gly255Ala
ENST00000373086.3:c.800G>C	ENSP00000362178.3:p.Gly267Ala
ENST00000373089.9:c.657G>C	ENSP00000362181.5:p.Trp219Cys