Canonical Allele Identifier: CA672885426

Gene: NRGN

Linked Data

• dbSNP Id: rs1489980521
• gnomAD v3: 11-124742207-G-A
• gnomAD v4: 11-124742207-G-A
• MyVariant Identifiers: chr11:g.124612103G>A (hg19) ; chr11:g.124742207G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.124742207G>A , CM000673.2:g.124742207G>A	GRCh38
NC_000011.9:g.124612103G>A , CM000673.1:g.124612103G>A	GRCh37
NC_000011.8:g.124117313G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000284292.11:c.15+2108G>A MANE Select	ENSP00000284292.5:n.15+2108G>A
ENST00000284292.10:c.15+2108G>A	ENSP00000284292.5:n.15+2108G>A
ENST00000412681.2:c.15+2108G>A	ENSP00000399591.1:n.15+2108G>A
NM_001126181.1:c.15+2108G>A	NP_001119653.1:n.15+2108G>A
NM_006176.2:c.15+2108G>A	NP_006167.1:n.15+2108G>A
XR_429013.2:n.2376C>T
XR_948129.1:n.1864C>T
XR_948130.1:n.1397C>T
XR_948131.1:n.2193C>T
NM_006176.3:c.15+2108G>A MANE Select	NP_006167.1:n.15+2108G>A
NM_001126181.2:c.15+2108G>A	NP_001119653.1:n.15+2108G>A