Canonical Allele Identifier: CA2334952020
Gene: SPINT2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38288100A= , CM000681.2:g.38288100A= GRCh38
NC_000019.9:g.38778740A= , CM000681.1:g.38778740A= GRCh37
NC_000019.8:g.43470580A= NCBI36
NG_013372.1:g.28643A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301244.12:c.337+165A= MANE Select ENSP00000301244.5:n.337+165A=
ENST00000301244.11:c.337+165A= ENSP00000301244.5:n.337+165A=
ENST00000454580.7:c.166+165A= ENSP00000389788.2:n.166+165A=
ENST00000587090.5:c.187+165A= ENSP00000466407.1:n.187+165A=
ENST00000587516.5:c.278-1038A= ENSP00000465721.1:n.278-1038A=
NM_001166103.1:c.166+165A= NP_001159575.1:n.166+165A=
NM_021102.3:c.337+165A= NP_066925.1:n.337+165A=
NM_021102.4:c.337+165A= MANE Select NP_066925.1:n.337+165A=
NM_001166103.2:c.166+165A= NP_001159575.1:n.166+165A=
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