Canonical Allele Identifier: CA672885443

Gene: NRGN

Linked Data

• dbSNP Id: rs1323949521
• gnomAD v3: 11-124742271-G-C
• gnomAD v4: 11-124742271-G-C
• MyVariant Identifiers: chr11:g.124612167G>C (hg19) ; chr11:g.124742271G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.124742271G>C , CM000673.2:g.124742271G>C	GRCh38
NC_000011.9:g.124612167G>C , CM000673.1:g.124612167G>C	GRCh37
NC_000011.8:g.124117377G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000284292.11:c.15+2172G>C MANE Select	ENSP00000284292.5:n.15+2172G>C
ENST00000284292.10:c.15+2172G>C	ENSP00000284292.5:n.15+2172G>C
ENST00000412681.2:c.15+2172G>C	ENSP00000399591.1:n.15+2172G>C
NM_001126181.1:c.15+2172G>C	NP_001119653.1:n.15+2172G>C
NM_006176.2:c.15+2172G>C	NP_006167.1:n.15+2172G>C
XR_429013.2:n.2312C>G
XR_948129.1:n.1800C>G
XR_948130.1:n.1333C>G
XR_948131.1:n.2129C>G
NM_006176.3:c.15+2172G>C MANE Select	NP_006167.1:n.15+2172G>C
NM_001126181.2:c.15+2172G>C	NP_001119653.1:n.15+2172G>C