Canonical Allele Identifier: CA346798823
Gene: SIX3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.44942175A>C , CM000664.2:g.44942175A>C GRCh38
NC_000002.11:g.45169314A>C , CM000664.1:g.45169314A>C GRCh37
NC_000002.10:g.45022818A>C NCBI36
NG_016222.1:g.5278A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260653.5:c.71A>C MANE Select ENSP00000260653.3:p.His24Pro
ENST00000260653.4:c.71A>C ENSP00000260653.3:p.His24Pro
NM_005413.3:c.71A>C NP_005404.1:p.His24Pro
XM_011533042.1:c.71A>C XP_011531344.1:p.His24Pro
NM_005413.4:c.71A>C MANE Select NP_005404.1:p.His24Pro