Canonical Allele Identifier: CA2584810792
Gene: SPINT2 HGNC NCBI

Linked Data

gnomAD v4: 19-38287995-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38287995A>G , CM000681.2:g.38287995A>G GRCh38
NC_000019.9:g.38778635A>G , CM000681.1:g.38778635A>G GRCh37
NC_000019.8:g.43470475A>G NCBI36
NG_013372.1:g.28538A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301244.12:c.337+60A>G MANE Select ENSP00000301244.5:n.337+60A>G
ENST00000301244.11:c.337+60A>G ENSP00000301244.5:n.337+60A>G
ENST00000454580.7:c.166+60A>G ENSP00000389788.2:n.166+60A>G
ENST00000587090.5:c.187+60A>G ENSP00000466407.1:n.187+60A>G
ENST00000587516.5:c.278-1143A>G ENSP00000465721.1:n.278-1143A>G
NM_001166103.1:c.166+60A>G NP_001159575.1:n.166+60A>G
NM_021102.3:c.337+60A>G NP_066925.1:n.337+60A>G
NM_021102.4:c.337+60A>G MANE Select NP_066925.1:n.337+60A>G
NM_001166103.2:c.166+60A>G NP_001159575.1:n.166+60A>G
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