Canonical Allele Identifier: CA2840376369
Gene: SHTN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117068039C>T , CM000672.2:g.117068039C>T GRCh38
NC_000010.10:g.118827550C>T , CM000672.1:g.118827550C>T GRCh37
NC_000010.9:g.118817540C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000392901.10:c.-188-19529G>A ENSP00000376635.4:n.-188-19529G>A
ENST00000392901.8:c.-188-19529G>A ENSP00000376635.4:n.-188-19529G>A
NM_001258300.1:c.-188-19529G>A NP_001245229.1:n.-188-19529G>A