Canonical Allele Identifier: CA882041411

Gene: SPINT2

Linked Data

• dbSNP Id: rs1429056480
• gnomAD v3: 19-38287753-T-C
• gnomAD v4: 19-38287753-T-C
• MyVariant Identifiers: chr19:g.38778393T>C (hg19) ; chr19:g.38287753T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38287753T>C , CM000681.2:g.38287753T>C	GRCh38
NC_000019.9:g.38778393T>C , CM000681.1:g.38778393T>C	GRCh37
NC_000019.8:g.43470233T>C	NCBI36
NG_013372.1:g.28296T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301244.12:c.278-123T>C MANE Select	ENSP00000301244.5:n.278-123T>C
ENST00000301244.11:c.278-123T>C	ENSP00000301244.5:n.278-123T>C
ENST00000454580.7:c.107-123T>C	ENSP00000389788.2:n.107-123T>C
ENST00000587090.5:c.128-123T>C	ENSP00000466407.1:n.128-123T>C
ENST00000587516.5:c.278-1385T>C	ENSP00000465721.1:n.278-1385T>C
ENST00000590210.1:n.475-123T>C
ENST00000590510.5:c.128-123T>C	ENSP00000465301.1:n.128-123T>C
ENST00000592007.1:c.128-123T>C	ENSP00000465561.1:n.128-123T>C
NM_001166103.1:c.107-123T>C	NP_001159575.1:n.107-123T>C
NM_021102.3:c.278-123T>C	NP_066925.1:n.278-123T>C
NM_021102.4:c.278-123T>C MANE Select	NP_066925.1:n.278-123T>C
NM_001166103.2:c.107-123T>C	NP_001159575.1:n.107-123T>C