Canonical Allele Identifier: CA426045571
Gene: SIX3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.45169258C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.44942119C>G , CM000664.2:g.44942119C>G GRCh38
NC_000002.11:g.45169258C>G , CM000664.1:g.45169258C>G GRCh37
NC_000002.10:g.45022762C>G NCBI36
NG_016222.1:g.5222C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000260653.5:c.15C>G MANE Select ENSP00000260653.3:p.Ser5=
ENST00000260653.4:c.15C>G ENSP00000260653.3:p.Ser5=
NM_005413.3:c.15C>G NP_005404.1:p.Ser5=
XM_011533042.1:c.15C>G XP_011531344.1:p.Ser5=
NM_005413.4:c.15C>G MANE Select NP_005404.1:p.Ser5=
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