Canonical Allele Identifier: CA2494534905
Gene: SIX3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.44942176C= , CM000664.2:g.44942176C= GRCh38
NC_000002.11:g.45169315C= , CM000664.1:g.45169315C= GRCh37
NC_000002.10:g.45022819C= NCBI36
NG_016222.1:g.5279C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260653.5:c.72C= MANE Select ENSP00000260653.3:p.His24=
ENST00000260653.4:c.72C= ENSP00000260653.3:p.His24=
NM_005413.3:c.72C= NP_005404.1:p.His24=
XM_011533042.1:c.72C= XP_011531344.1:p.His24=
NM_005413.4:c.72C= MANE Select NP_005404.1:p.His24=
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