Canonical Allele Identifier: CA346798987
Gene: SIX3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.44942260C>A , CM000664.2:g.44942260C>A GRCh38
NC_000002.11:g.45169399C>A , CM000664.1:g.45169399C>A GRCh37
NC_000002.10:g.45022903C>A NCBI36
NG_016222.1:g.5363C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260653.5:c.156C>A MANE Select ENSP00000260653.3:p.Asn52Lys
ENST00000260653.4:c.156C>A ENSP00000260653.3:p.Asn52Lys
NM_005413.3:c.156C>A NP_005404.1:p.Asn52Lys
XM_011533042.1:c.156C>A XP_011531344.1:p.Asn52Lys
NM_005413.4:c.156C>A MANE Select NP_005404.1:p.Asn52Lys