Canonical Allele Identifier: CA230377000
Gene: NRGN HGNC NCBI

Linked Data

dbSNP Id: rs994940978
MyVariant Identifiers: chr11:g.124612060G>C (hg19) chr11:g.124742164G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.124742164G>C , CM000673.2:g.124742164G>C GRCh38
NC_000011.9:g.124612060G>C , CM000673.1:g.124612060G>C GRCh37
NC_000011.8:g.124117270G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000284292.11:c.15+2065G>C MANE Select ENSP00000284292.5:n.15+2065G>C
ENST00000284292.10:c.15+2065G>C ENSP00000284292.5:n.15+2065G>C
ENST00000412681.2:c.15+2065G>C ENSP00000399591.1:n.15+2065G>C
NM_001126181.1:c.15+2065G>C NP_001119653.1:n.15+2065G>C
NM_006176.2:c.15+2065G>C NP_006167.1:n.15+2065G>C
XR_429013.2:n.2419C>G
XR_948129.1:n.1907C>G
XR_948130.1:n.1440C>G
XR_948131.1:n.2236C>G
NM_006176.3:c.15+2065G>C MANE Select NP_006167.1:n.15+2065G>C
NM_001126181.2:c.15+2065G>C NP_001119653.1:n.15+2065G>C
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