Canonical Allele Identifier: CA2737131375
Gene: NTSR1 HGNC NCBI

Linked Data

dbSNP Id: rs2147141177
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.62738020A>G , CM000682.2:g.62738020A>G GRCh38
NC_000020.10:g.61369372A>G , CM000682.1:g.61369372A>G GRCh37
NC_000020.9:g.60839817A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000370501.4:c.715-16665A>G MANE Select ENSP00000359532.3:n.715-16665A>G
ENST00000370501.3:c.715-16665A>G ENSP00000359532.3:n.715-16665A>G
NM_002531.2:c.715-16665A>G NP_002522.2:n.715-16665A>G
XM_011528827.1:c.715-16665A>G XP_011527129.1:n.715-16665A>G
XM_011528827.2:c.715-16665A>G XP_011527129.1:n.715-16665A>G
NM_002531.3:c.715-16665A>G MANE Select NP_002522.2:n.715-16665A>G
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