Canonical Allele Identifier: CA653835838

Gene: SHTN1

Linked Data

• dbSNP Id: rs1853028859
• COSMIC: COSN24492810

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.117068075C>A , CM000672.2:g.117068075C>A	GRCh38
NC_000010.10:g.118827586C>A , CM000672.1:g.118827586C>A	GRCh37
NC_000010.9:g.118817576C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000392901.10:c.-188-19565G>T	ENSP00000376635.4:n.-188-19565G>T
ENST00000392901.8:c.-188-19565G>T	ENSP00000376635.4:n.-188-19565G>T
NM_001258300.1:c.-188-19565G>T	NP_001245229.1:n.-188-19565G>T