Canonical Allele Identifier: CA507961311
Gene: SIX5 HGNC NCBI

Linked Data

gnomAD v4: 19-45766552-G-T
MyVariant Identifiers: chr19:g.46269810G>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45766552G>T , CM000681.2:g.45766552G>T GRCh38
NC_000019.9:g.46269810G>T , CM000681.1:g.46269810G>T GRCh37
NC_000019.8:g.50961650G>T NCBI36
NG_012745.1:g.7688C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000317578.7:c.1407C>A MANE Select ENSP00000316842.4:p.Thr469=
ENST00000317578.6:c.1407C>A ENSP00000316842.4:p.Thr469=
ENST00000560160.1:c.587-441C>A
ENST00000560168.1:c.*595C>A ENSP00000453189.2:n.*595C>A
ENST00000622857.1:c.16-590C>A ENSP00000481365.1:n.16-590C>A
NM_175875.4:c.1407C>A NP_787071.2:p.Thr469=
NM_175875.5:c.1407C>A MANE Select NP_787071.3:p.Thr469=
Search 100 bp 5'
Search 100 bp 3'