Canonical Allele Identifier: CA3499079
Gene: SH3TC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 763367
ClinVar RCV Id: RCV000941601
dbSNP Id: rs751912297

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149027737G>A , CM000667.2:g.149027737G>A GRCh38
NC_000005.9:g.148407300G>A , CM000667.1:g.148407300G>A GRCh37
NC_000005.8:g.148387493G>A NCBI36
NG_007947.2:g.40438C>T , LRG_269:g.40438C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000502274.2:c.1891C>T
ENST00000515425.6:c.1995C>T MANE Select ENSP00000423660.1:p.His665=
ENST00000675793.1:c.*1279C>T ENSP00000502039.1:n.*1279C>T
ENST00000676056.1:c.*1505C>T ENSP00000501827.1:n.*1505C>T
ENST00000323829.9:c.*1383C>T ENSP00000313025.5:n.*1383C>T
ENST00000504517.5:c.1525C>T ENSP00000421779.1:n.1525C>T
ENST00000504690.5:c.1995C>T ENSP00000425627.1:p.His665=
ENST00000510779.1:c.1045C>T
ENST00000511307.5:c.*1775C>T ENSP00000421420.1:n.*1775C>T
ENST00000512049.5:c.1974C>T ENSP00000421860.1:p.His658=
ENST00000513604.5:c.*1383C>T ENSP00000423111.1:n.*1383C>T
ENST00000515425.5:c.1995C>T ENSP00000423660.1:p.His665=
NM_024577.3:c.1995C>T , LRG_269t1:c.1995C>T NP_078853.2:p.His665=
NM_024577.4:c.1995C>T MANE Select NP_078853.2:p.His665=