Canonical Allele Identifier: CA1590328096

Gene: SH3TC2

Linked Data

• dbSNP Id: rs1580924339

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149062903T>C , CM000667.2:g.149062903T>C	GRCh38
NC_000005.9:g.148442466T>C , CM000667.1:g.148442466T>C	GRCh37
NC_000005.8:g.148422659T>C	NCBI36
NG_007947.2:g.5272A>G , LRG_269:g.5272A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000515425.6:c.52+68A>G MANE Select	ENSP00000423660.1:n.52+68A>G
ENST00000674983.1:c.52+68A>G	ENSP00000502387.1:n.52+68A>G
ENST00000675793.1:c.52+68A>G	ENSP00000502039.1:n.52+68A>G
ENST00000676056.1:c.52+68A>G	ENSP00000501827.1:n.52+68A>G
ENST00000323829.9:c.52+68A>G	ENSP00000313025.5:n.52+68A>G
ENST00000504091.1:n.88+68A>G
ENST00000504690.5:c.52+68A>G	ENSP00000425627.1:n.52+68A>G
ENST00000511307.5:c.52+68A>G	ENSP00000421420.1:n.52+68A>G
ENST00000511949.5:n.92+68A>G
ENST00000512049.5:c.52+68A>G	ENSP00000421860.1:n.52+68A>G
ENST00000513604.5:c.52+68A>G	ENSP00000423111.1:n.52+68A>G
ENST00000515425.5:c.52+68A>G	ENSP00000423660.1:n.52+68A>G
NM_024577.3:c.52+68A>G , LRG_269t1:c.52+68A>G	NP_078853.2:n.52+68A>G
NM_024577.4:c.52+68A>G MANE Select	NP_078853.2:n.52+68A>G