Canonical Allele Identifier: CA2334951977
Gene: SPINT2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38288010G= , CM000681.2:g.38288010G= GRCh38
NC_000019.9:g.38778650G= , CM000681.1:g.38778650G= GRCh37
NC_000019.8:g.43470490G= NCBI36
NG_013372.1:g.28553G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301244.12:c.337+75G= MANE Select ENSP00000301244.5:n.337+75G=
ENST00000301244.11:c.337+75G= ENSP00000301244.5:n.337+75G=
ENST00000454580.7:c.166+75G= ENSP00000389788.2:n.166+75G=
ENST00000587090.5:c.187+75G= ENSP00000466407.1:n.187+75G=
ENST00000587516.5:c.278-1128G= ENSP00000465721.1:n.278-1128G=
NM_001166103.1:c.166+75G= NP_001159575.1:n.166+75G=
NM_021102.3:c.337+75G= NP_066925.1:n.337+75G=
NM_021102.4:c.337+75G= MANE Select NP_066925.1:n.337+75G=
NM_001166103.2:c.166+75G= NP_001159575.1:n.166+75G=
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