Canonical Allele Identifier: CA1590297836
Gene: SH3TC2 HGNC NCBI

Linked Data

dbSNP Id: rs1753477178
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148994678A>G , CM000667.2:g.148994678A>G GRCh38
NC_000005.9:g.148374241A>G , CM000667.1:g.148374241A>G GRCh37
NC_000005.8:g.148354434A>G NCBI36
NG_007947.2:g.73497T>C , LRG_269:g.73497T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000515425.6:c.*10033T>C MANE Select ENSP00000423660.1:n.*10033T>C
ENST00000504690.5:c.*12+9048T>C ENSP00000425627.1:n.*12+9048T>C
ENST00000510350.1:n.231+12203T>C
NM_024577.3:c.*10033T>C , LRG_269t1:c.*10033T>C NP_078853.2:n.*10033T>C
NM_024577.4:c.*10033T>C MANE Select NP_078853.2:n.*10033T>C
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