Canonical Allele Identifier: CA2334952023
Gene: SPINT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38288114G= , CM000681.2:g.38288114G= GRCh38
NC_000019.9:g.38778754G= , CM000681.1:g.38778754G= GRCh37
NC_000019.8:g.43470594G= NCBI36
NG_013372.1:g.28657G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301244.12:c.337+179G= MANE Select ENSP00000301244.5:n.337+179G=
ENST00000301244.11:c.337+179G= ENSP00000301244.5:n.337+179G=
ENST00000454580.7:c.166+179G= ENSP00000389788.2:n.166+179G=
ENST00000587090.5:c.187+179G= ENSP00000466407.1:n.187+179G=
ENST00000587516.5:c.278-1024G= ENSP00000465721.1:n.278-1024G=
NM_001166103.1:c.166+179G= NP_001159575.1:n.166+179G=
NM_021102.3:c.337+179G= NP_066925.1:n.337+179G=
NM_021102.4:c.337+179G= MANE Select NP_066925.1:n.337+179G=
NM_001166103.2:c.166+179G= NP_001159575.1:n.166+179G=