Canonical Allele Identifier: CA346798885
Gene: SIX3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.44942207G>T , CM000664.2:g.44942207G>T GRCh38
NC_000002.11:g.45169346G>T , CM000664.1:g.45169346G>T GRCh37
NC_000002.10:g.45022850G>T NCBI36
NG_016222.1:g.5310G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000260653.5:c.103G>T MANE Select ENSP00000260653.3:p.Gly35Trp
ENST00000260653.4:c.103G>T ENSP00000260653.3:p.Gly35Trp
NM_005413.3:c.103G>T NP_005404.1:p.Gly35Trp
XM_011533042.1:c.103G>T XP_011531344.1:p.Gly35Trp
NM_005413.4:c.103G>T MANE Select NP_005404.1:p.Gly35Trp