Canonical Allele Identifier: CA1939014522
Gene: SHTN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117067976G= , CM000672.2:g.117067976G= GRCh38
NC_000010.10:g.118827487G= , CM000672.1:g.118827487G= GRCh37
NC_000010.9:g.118817477G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000392901.10:c.-188-19466C= ENSP00000376635.4:n.-188-19466C=
ENST00000392901.8:c.-188-19466C= ENSP00000376635.4:n.-188-19466C=
NM_001258300.1:c.-188-19466C= NP_001245229.1:n.-188-19466C=