Canonical Allele Identifier: CA805483627
Gene: SH3TC2 HGNC NCBI

Linked Data

dbSNP Id: rs1429884387

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148994576G>A , CM000667.2:g.148994576G>A GRCh38
NC_000005.9:g.148374139G>A , CM000667.1:g.148374139G>A GRCh37
NC_000005.8:g.148354332G>A NCBI36
NG_007947.2:g.73599C>T , LRG_269:g.73599C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000515425.6:c.*10135C>T MANE Select ENSP00000423660.1:n.*10135C>T
ENST00000504690.5:c.*12+9150C>T ENSP00000425627.1:n.*12+9150C>T
ENST00000510350.1:n.231+12305C>T
NM_024577.3:c.*10135C>T , LRG_269t1:c.*10135C>T NP_078853.2:n.*10135C>T
NM_024577.4:c.*10135C>T MANE Select NP_078853.2:n.*10135C>T