Canonical Allele Identifier: CA507219249

Gene: SPINT2

Linked Data

• gnomAD v4: 19-38287922-C-G
• MyVariant Identifiers: chr19:g.38778562C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38287922C>G , CM000681.2:g.38287922C>G	GRCh38
NC_000019.9:g.38778562C>G , CM000681.1:g.38778562C>G	GRCh37
NC_000019.8:g.43470402C>G	NCBI36
NG_013372.1:g.28465C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301244.12:c.324C>G MANE Select	ENSP00000301244.5:p.Ser108=
ENST00000301244.11:c.324C>G	ENSP00000301244.5:p.Ser108=
ENST00000454580.7:c.153C>G	ENSP00000389788.2:p.Ser51=
ENST00000587090.5:c.174C>G	ENSP00000466407.1:p.Ser58=
ENST00000587516.5:c.278-1216C>G	ENSP00000465721.1:n.278-1216C>G
ENST00000590210.1:n.521C>G
ENST00000592007.1:c.174C>G	ENSP00000465561.1:p.Ser58=
NM_001166103.1:c.153C>G	NP_001159575.1:p.Ser51=
NM_021102.3:c.324C>G	NP_066925.1:p.Ser108=
NM_021102.4:c.324C>G MANE Select	NP_066925.1:p.Ser108=
NM_001166103.2:c.153C>G	NP_001159575.1:p.Ser51=