Canonical Allele Identifier: CA448963109
Gene: NRSN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.24145898T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24145670T>C , CM000668.2:g.24145670T>C GRCh38
NC_000006.11:g.24145898T>C , CM000668.1:g.24145898T>C GRCh37
NC_000006.10:g.24253877T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000378491.9:c.312T>C MANE Select ENSP00000367752.4:p.His104=
ENST00000378477.2:c.312T>C ENSP00000367738.2:p.His104=
ENST00000378478.5:c.312T>C ENSP00000367739.2:p.His104=
ENST00000378491.8:c.312T>C ENSP00000367752.4:p.His104=
ENST00000468195.2:n.257-9101T>C
NM_080723.4:c.312T>C NP_542454.3:p.His104=
NM_080723.5:c.312T>C MANE Select NP_542454.3:p.His104=