Canonical Allele Identifier: CA823266091
Gene: NRSN1 HGNC NCBI

Linked Data

dbSNP Id: rs1370764990
gnomAD v3: 6-24146007-A-G
gnomAD v4: 6-24146007-A-G
MyVariant Identifiers: chr6:g.24146235A>G (hg19) chr6:g.24146007A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24146007A>G , CM000668.2:g.24146007A>G GRCh38
NC_000006.11:g.24146235A>G , CM000668.1:g.24146235A>G GRCh37
NC_000006.10:g.24254214A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000378491.9:c.*61A>G MANE Select ENSP00000367752.4:n.*61A>G
ENST00000378478.5:c.*61A>G ENSP00000367739.2:n.*61A>G
ENST00000378491.8:c.*61A>G ENSP00000367752.4:n.*61A>G
ENST00000468195.2:n.257-8764A>G
NM_080723.4:c.*61A>G NP_542454.3:n.*61A>G
NM_080723.5:c.*61A>G MANE Select NP_542454.3:n.*61A>G
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