Canonical Allele Identifier: CA426045569
Gene: SIX3 HGNC NCBI

Linked Data

dbSNP Id: rs1349264486
MyVariant Identifiers: chr2:g.45169255C>T (hg19) chr2:g.44942116C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.44942116C>T , CM000664.2:g.44942116C>T GRCh38
NC_000002.11:g.45169255C>T , CM000664.1:g.45169255C>T GRCh37
NC_000002.10:g.45022759C>T NCBI36
NG_016222.1:g.5219C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000260653.5:c.12C>T MANE Select ENSP00000260653.3:p.Arg4=
ENST00000260653.4:c.12C>T ENSP00000260653.3:p.Arg4=
NM_005413.3:c.12C>T NP_005404.1:p.Arg4=
XM_011533042.1:c.12C>T XP_011531344.1:p.Arg4=
NM_005413.4:c.12C>T MANE Select NP_005404.1:p.Arg4=
Search 100 bp 5'
Search 100 bp 3'