Canonical Allele Identifier: CA2334952058
Gene: SPINT2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38288186G= , CM000681.2:g.38288186G= GRCh38
NC_000019.9:g.38778826G= , CM000681.1:g.38778826G= GRCh37
NC_000019.8:g.43470666G= NCBI36
NG_013372.1:g.28729G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301244.12:c.337+251G= MANE Select ENSP00000301244.5:n.337+251G=
ENST00000301244.11:c.337+251G= ENSP00000301244.5:n.337+251G=
ENST00000454580.7:c.166+251G= ENSP00000389788.2:n.166+251G=
ENST00000587090.5:c.187+251G= ENSP00000466407.1:n.187+251G=
ENST00000587516.5:c.278-952G= ENSP00000465721.1:n.278-952G=
NM_001166103.1:c.166+251G= NP_001159575.1:n.166+251G=
NM_021102.3:c.337+251G= NP_066925.1:n.337+251G=
NM_021102.4:c.337+251G= MANE Select NP_066925.1:n.337+251G=
NM_001166103.2:c.166+251G= NP_001159575.1:n.166+251G=
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