Canonical Allele Identifier: CA1590297661
Gene: SH3TC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148994470C= , CM000667.2:g.148994470C= GRCh38
NC_000005.9:g.148374033C= , CM000667.1:g.148374033C= GRCh37
NC_000005.8:g.148354226C= NCBI36
NG_007947.2:g.73705G= , LRG_269:g.73705G=

Transcript Alleles

HGVS Amino-acid change
ENST00000515425.6:c.*10241G= MANE Select ENSP00000423660.1:n.*10241G=
ENST00000504690.5:c.*12+9256G= ENSP00000425627.1:n.*12+9256G=
ENST00000510350.1:n.231+12411G=
NM_024577.3:c.*10241G= , LRG_269t1:c.*10241G= NP_078853.2:n.*10241G=
NM_024577.4:c.*10241G= MANE Select NP_078853.2:n.*10241G=