Canonical Allele Identifier: CA805483648
Gene: SH3TC2 HGNC NCBI

Linked Data

dbSNP Id: rs943889013

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148994600A>T , CM000667.2:g.148994600A>T GRCh38
NC_000005.9:g.148374163A>T , CM000667.1:g.148374163A>T GRCh37
NC_000005.8:g.148354356A>T NCBI36
NG_007947.2:g.73575T>A , LRG_269:g.73575T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000515425.6:c.*10111T>A MANE Select ENSP00000423660.1:n.*10111T>A
ENST00000504690.5:c.*12+9126T>A ENSP00000425627.1:n.*12+9126T>A
ENST00000510350.1:n.231+12281T>A
NM_024577.3:c.*10111T>A , LRG_269t1:c.*10111T>A NP_078853.2:n.*10111T>A
NM_024577.4:c.*10111T>A MANE Select NP_078853.2:n.*10111T>A