Canonical Allele Identifier: CA230377043

Gene: NRGN

Linked Data

• dbSNP Id: rs968968970
• MyVariant Identifiers: chr11:g.124612175T>G (hg19) ; chr11:g.124742279T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.124742279T>G , CM000673.2:g.124742279T>G	GRCh38
NC_000011.9:g.124612175T>G , CM000673.1:g.124612175T>G	GRCh37
NC_000011.8:g.124117385T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000284292.11:c.15+2180T>G MANE Select	ENSP00000284292.5:n.15+2180T>G
ENST00000284292.10:c.15+2180T>G	ENSP00000284292.5:n.15+2180T>G
ENST00000412681.2:c.15+2180T>G	ENSP00000399591.1:n.15+2180T>G
NM_001126181.1:c.15+2180T>G	NP_001119653.1:n.15+2180T>G
NM_006176.2:c.15+2180T>G	NP_006167.1:n.15+2180T>G
XR_429013.2:n.2304A>C
XR_948129.1:n.1792A>C
XR_948130.1:n.1325A>C
XR_948131.1:n.2121A>C
NM_006176.3:c.15+2180T>G MANE Select	NP_006167.1:n.15+2180T>G
NM_001126181.2:c.15+2180T>G	NP_001119653.1:n.15+2180T>G