Canonical Allele Identifier: CA1939014514

Gene: SHTN1

Linked Data

• dbSNP Id: rs1853026864

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.117067967T>G , CM000672.2:g.117067967T>G	GRCh38
NC_000010.10:g.118827478T>G , CM000672.1:g.118827478T>G	GRCh37
NC_000010.9:g.118817468T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000392901.10:c.-188-19457A>C	ENSP00000376635.4:n.-188-19457A>C
ENST00000392901.8:c.-188-19457A>C	ENSP00000376635.4:n.-188-19457A>C
NM_001258300.1:c.-188-19457A>C	NP_001245229.1:n.-188-19457A>C