Canonical Allele Identifier: CA346800352
Gene: SIX3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.45170024G>C (hg19) chr2:g.44942885G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.44942885G>C , CM000664.2:g.44942885G>C GRCh38
NC_000002.11:g.45170024G>C , CM000664.1:g.45170024G>C GRCh37
NC_000002.10:g.45023528G>C NCBI36
NG_016222.1:g.5988G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000260653.5:c.781G>C MANE Select ENSP00000260653.3:p.Asp261His
ENST00000260653.4:c.781G>C ENSP00000260653.3:p.Asp261His
NM_005413.3:c.781G>C NP_005404.1:p.Asp261His
XM_011533042.1:c.781G>C XP_011531344.1:p.Asp261His
NM_005413.4:c.781G>C MANE Select NP_005404.1:p.Asp261His
Search 100 bp 5'
Search 100 bp 3'