Canonical Allele Identifier: CA805483594
Gene: SH3TC2 HGNC NCBI

Linked Data

dbSNP Id: rs1170017543
MyVariant Identifiers: chr5:g.148374034A>T (hg19) chr5:g.148994471A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148994471A>T , CM000667.2:g.148994471A>T GRCh38
NC_000005.9:g.148374034A>T , CM000667.1:g.148374034A>T GRCh37
NC_000005.8:g.148354227A>T NCBI36
NG_007947.2:g.73704T>A , LRG_269:g.73704T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000515425.6:c.*10240T>A MANE Select ENSP00000423660.1:n.*10240T>A
ENST00000504690.5:c.*12+9255T>A ENSP00000425627.1:n.*12+9255T>A
ENST00000510350.1:n.231+12410T>A
NM_024577.3:c.*10240T>A , LRG_269t1:c.*10240T>A NP_078853.2:n.*10240T>A
NM_024577.4:c.*10240T>A MANE Select NP_078853.2:n.*10240T>A
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