Canonical Allele Identifier: CA1642233
Gene: SIX3 HGNC NCBI

Linked Data

dbSNP Id: rs763869939
ExAC: 2:45169258 C / T
gnomAD v2: 2-45169258-C-T
gnomAD v3: 2-44942119-C-T
gnomAD v4: 2-44942119-C-T
MyVariant Identifiers: chr2:g.45169258C>T (hg19) chr2:g.44942119C>T (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000260653.5:c.15C>T MANE Select ENSP00000260653.3:p.Ser5=
ENST00000260653.4:c.15C>T ENSP00000260653.3:p.Ser5=
NM_005413.3:c.15C>T NP_005404.1:p.Ser5=
XM_011533042.1:c.15C>T XP_011531344.1:p.Ser5=
NM_005413.4:c.15C>T MANE Select NP_005404.1:p.Ser5=
Search 100 bp 5'
Search 100 bp 3'