Canonical Allele Identifier: CA507961217
Gene: SIX5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.46269732C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45766474C>T , CM000681.2:g.45766474C>T GRCh38
NC_000019.9:g.46269732C>T , CM000681.1:g.46269732C>T GRCh37
NC_000019.8:g.50961572C>T NCBI36
NG_012745.1:g.7766G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000317578.7:c.1485G>A MANE Select ENSP00000316842.4:p.Gln495=
ENST00000317578.6:c.1485G>A ENSP00000316842.4:p.Gln495=
ENST00000560160.1:c.587-363G>A
ENST00000560168.1:c.*673G>A ENSP00000453189.2:n.*673G>A
ENST00000622857.1:c.16-512G>A ENSP00000481365.1:n.16-512G>A
NM_175875.4:c.1485G>A NP_787071.2:p.Gln495=
NM_175875.5:c.1485G>A MANE Select NP_787071.3:p.Gln495=
Search 100 bp 5'
Search 100 bp 3'