Canonical Allele Identifier: CA2736063889

Gene: SPINT2

Linked Data

• dbSNP Id: rs2146277738

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38287705G>C , CM000681.2:g.38287705G>C	GRCh38
NC_000019.9:g.38778345G>C , CM000681.1:g.38778345G>C	GRCh37
NC_000019.8:g.43470185G>C	NCBI36
NG_013372.1:g.28248G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301244.12:c.278-171G>C MANE Select	ENSP00000301244.5:n.278-171G>C
ENST00000301244.11:c.278-171G>C	ENSP00000301244.5:n.278-171G>C
ENST00000454580.7:c.107-171G>C	ENSP00000389788.2:n.107-171G>C
ENST00000587090.5:c.128-171G>C	ENSP00000466407.1:n.128-171G>C
ENST00000587516.5:c.278-1433G>C	ENSP00000465721.1:n.278-1433G>C
ENST00000590210.1:n.475-171G>C
ENST00000590510.5:c.128-171G>C	ENSP00000465301.1:n.128-171G>C
ENST00000592007.1:c.128-171G>C	ENSP00000465561.1:n.128-171G>C
NM_001166103.1:c.107-171G>C	NP_001159575.1:n.107-171G>C
NM_021102.3:c.278-171G>C	NP_066925.1:n.278-171G>C
NM_021102.4:c.278-171G>C MANE Select	NP_066925.1:n.278-171G>C
NM_001166103.2:c.107-171G>C	NP_001159575.1:n.107-171G>C