Canonical Allele Identifier: CA2140897388
Gene: SIX1 HGNC NCBI

Linked Data

dbSNP Id: rs1894922935
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60645484T>C , CM000676.2:g.60645484T>C GRCh38
NC_000014.8:g.61112202T>C , CM000676.1:g.61112202T>C GRCh37
NC_000014.7:g.60181955T>C NCBI36
NG_008231.1:g.8954A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000645694.3:c.*799A>G MANE Select ENSP00000494686.1:n.*799A>G
ENST00000247182.6:c.*799A>G ENSP00000247182.5:n.*799A>G
ENST00000553535.2:n.1342A>G
ENST00000554986.2:c.*799A>G ENSP00000452700.2:n.*799A>G
ENST00000555955.3:n.2291A>G
NM_005982.3:c.*799A>G NP_005973.1:n.*799A>G
XM_017021602.2:c.*1073A>G XP_016877091.1:n.*1073A>G
NM_005982.4:c.*799A>G MANE Select NP_005973.1:n.*799A>G
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