Canonical Allele Identifier: CA1590297819
Gene: SH3TC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148994659G= , CM000667.2:g.148994659G= GRCh38
NC_000005.9:g.148374222G= , CM000667.1:g.148374222G= GRCh37
NC_000005.8:g.148354415G= NCBI36
NG_007947.2:g.73516C= , LRG_269:g.73516C=

Transcript Alleles

HGVS Amino-acid change
ENST00000515425.6:c.*10052C= MANE Select ENSP00000423660.1:n.*10052C=
ENST00000504690.5:c.*12+9067C= ENSP00000425627.1:n.*12+9067C=
ENST00000510350.1:n.231+12222C=
NM_024577.3:c.*10052C= , LRG_269t1:c.*10052C= NP_078853.2:n.*10052C=
NM_024577.4:c.*10052C= MANE Select NP_078853.2:n.*10052C=