Canonical Allele Identifier: CA2006335584

Gene: NRGN

Linked Data

• dbSNP Id: rs12278912

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.124742263G>T , CM000673.2:g.124742263G>T	GRCh38
NC_000011.9:g.124612159G>T , CM000673.1:g.124612159G>T	GRCh37
NC_000011.8:g.124117369G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000284292.11:c.15+2164G>T MANE Select	ENSP00000284292.5:n.15+2164G>T
ENST00000284292.10:c.15+2164G>T	ENSP00000284292.5:n.15+2164G>T
ENST00000412681.2:c.15+2164G>T	ENSP00000399591.1:n.15+2164G>T
NM_001126181.1:c.15+2164G>T	NP_001119653.1:n.15+2164G>T
NM_006176.2:c.15+2164G>T	NP_006167.1:n.15+2164G>T
XR_429013.2:n.2320C>A
XR_948129.1:n.1808C>A
XR_948130.1:n.1341C>A
XR_948131.1:n.2137C>A
NM_006176.3:c.15+2164G>T MANE Select	NP_006167.1:n.15+2164G>T
NM_001126181.2:c.15+2164G>T	NP_001119653.1:n.15+2164G>T