Canonical Allele Identifier: CA214957656
Gene: SHTN1 HGNC NCBI

Linked Data

dbSNP Id: rs563044797

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117068080G>A , CM000672.2:g.117068080G>A GRCh38
NC_000010.10:g.118827591G>A , CM000672.1:g.118827591G>A GRCh37
NC_000010.9:g.118817581G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000392901.10:c.-188-19570C>T ENSP00000376635.4:n.-188-19570C>T
ENST00000392901.8:c.-188-19570C>T ENSP00000376635.4:n.-188-19570C>T
NM_001258300.1:c.-188-19570C>T NP_001245229.1:n.-188-19570C>T