Canonical Allele Identifier: CA1590297646

Gene: SH3TC2

Linked Data

• dbSNP Id: rs1580879941

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148994433G>A , CM000667.2:g.148994433G>A	GRCh38
NC_000005.9:g.148373996G>A , CM000667.1:g.148373996G>A	GRCh37
NC_000005.8:g.148354189G>A	NCBI36
NG_007947.2:g.73742C>T , LRG_269:g.73742C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000515425.6:c.*10278C>T MANE Select	ENSP00000423660.1:n.*10278C>T
ENST00000504690.5:c.*12+9293C>T	ENSP00000425627.1:n.*12+9293C>T
ENST00000510350.1:n.231+12448C>T
NM_024577.3:c.*10278C>T , LRG_269t1:c.*10278C>T	NP_078853.2:n.*10278C>T
NM_024577.4:c.*10278C>T MANE Select	NP_078853.2:n.*10278C>T