Canonical Allele Identifier: CA426045589
Gene: SIX3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.45169294A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.44942155A>C , CM000664.2:g.44942155A>C GRCh38
NC_000002.11:g.45169294A>C , CM000664.1:g.45169294A>C GRCh37
NC_000002.10:g.45022798A>C NCBI36
NG_016222.1:g.5258A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260653.5:c.51A>C MANE Select ENSP00000260653.3:p.Pro17=
ENST00000260653.4:c.51A>C ENSP00000260653.3:p.Pro17=
NM_005413.3:c.51A>C NP_005404.1:p.Pro17=
XM_011533042.1:c.51A>C XP_011531344.1:p.Pro17=
NM_005413.4:c.51A>C MANE Select NP_005404.1:p.Pro17=
Search 100 bp 5'
Search 100 bp 3'