Canonical Allele Identifier: CA660437238
Gene: SHTN1 HGNC NCBI

Linked Data

dbSNP Id: rs1174880379

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117068066C>G , CM000672.2:g.117068066C>G GRCh38
NC_000010.10:g.118827577C>G , CM000672.1:g.118827577C>G GRCh37
NC_000010.9:g.118817567C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000392901.10:c.-188-19556G>C ENSP00000376635.4:n.-188-19556G>C
ENST00000392901.8:c.-188-19556G>C ENSP00000376635.4:n.-188-19556G>C
NM_001258300.1:c.-188-19556G>C NP_001245229.1:n.-188-19556G>C