Canonical Allele Identifier: CA2494535126
Gene: SIX3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.44942312T= , CM000664.2:g.44942312T= GRCh38
NC_000002.11:g.45169451T= , CM000664.1:g.45169451T= GRCh37
NC_000002.10:g.45022955T= NCBI36
NG_016222.1:g.5415T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260653.5:c.208T= MANE Select ENSP00000260653.3:p.Ser70=
ENST00000260653.4:c.208T= ENSP00000260653.3:p.Ser70=
NM_005413.3:c.208T= NP_005404.1:p.Ser70=
XM_011533042.1:c.208T= XP_011531344.1:p.Ser70=
NM_005413.4:c.208T= MANE Select NP_005404.1:p.Ser70=
Search 100 bp 5'
Search 100 bp 3'