Canonical Allele Identifier: CA2584810894

Gene: SPINT2

Linked Data

• gnomAD v4: 19-38288129-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38288129C>G , CM000681.2:g.38288129C>G	GRCh38
NC_000019.9:g.38778769C>G , CM000681.1:g.38778769C>G	GRCh37
NC_000019.8:g.43470609C>G	NCBI36
NG_013372.1:g.28672C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301244.12:c.337+194C>G MANE Select	ENSP00000301244.5:n.337+194C>G
ENST00000301244.11:c.337+194C>G	ENSP00000301244.5:n.337+194C>G
ENST00000454580.7:c.166+194C>G	ENSP00000389788.2:n.166+194C>G
ENST00000587090.5:c.187+194C>G	ENSP00000466407.1:n.187+194C>G
ENST00000587516.5:c.278-1009C>G	ENSP00000465721.1:n.278-1009C>G
NM_001166103.1:c.166+194C>G	NP_001159575.1:n.166+194C>G
NM_021102.3:c.337+194C>G	NP_066925.1:n.337+194C>G
NM_021102.4:c.337+194C>G MANE Select	NP_066925.1:n.337+194C>G
NM_001166103.2:c.166+194C>G	NP_001159575.1:n.166+194C>G