Canonical Allele Identifier: CA317319581
Gene: NTSR1 HGNC NCBI

Linked Data

dbSNP Id: rs201959254
gnomAD v3: 20-62738021-A-C
gnomAD v4: 20-62738021-A-C
MyVariant Identifiers: chr20:g.61369373A>C (hg19) chr20:g.62738021A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.62738021A>C , CM000682.2:g.62738021A>C GRCh38
NC_000020.10:g.61369373A>C , CM000682.1:g.61369373A>C GRCh37
NC_000020.9:g.60839818A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000370501.4:c.715-16664A>C MANE Select ENSP00000359532.3:n.715-16664A>C
ENST00000370501.3:c.715-16664A>C ENSP00000359532.3:n.715-16664A>C
NM_002531.2:c.715-16664A>C NP_002522.2:n.715-16664A>C
XM_011528827.1:c.715-16664A>C XP_011527129.1:n.715-16664A>C
XM_011528827.2:c.715-16664A>C XP_011527129.1:n.715-16664A>C
NM_002531.3:c.715-16664A>C MANE Select NP_002522.2:n.715-16664A>C
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