Canonical Allele Identifier: CA1939014518
Gene: SHTN1 HGNC NCBI

Linked Data

dbSNP Id: rs1853027000

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117067970A>C , CM000672.2:g.117067970A>C GRCh38
NC_000010.10:g.118827481A>C , CM000672.1:g.118827481A>C GRCh37
NC_000010.9:g.118817471A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000392901.10:c.-188-19460T>G ENSP00000376635.4:n.-188-19460T>G
ENST00000392901.8:c.-188-19460T>G ENSP00000376635.4:n.-188-19460T>G
NM_001258300.1:c.-188-19460T>G NP_001245229.1:n.-188-19460T>G