Canonical Allele Identifier: CA406421119
Gene: SIX5 HGNC NCBI

Linked Data

gnomAD v4: 19-45767064-C-T
MyVariant Identifiers: chr19:g.46270322C>T (hg19) chr19:g.45767064C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45767064C>T , CM000681.2:g.45767064C>T GRCh38
NC_000019.9:g.46270322C>T , CM000681.1:g.46270322C>T GRCh37
NC_000019.8:g.50962162C>T NCBI36
NG_012745.1:g.7176G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000317578.7:c.895G>A MANE Select ENSP00000316842.4:p.Ala299Thr
ENST00000317578.6:c.895G>A ENSP00000316842.4:p.Ala299Thr
ENST00000560160.1:c.587-953G>A
ENST00000560168.1:c.*83G>A ENSP00000453189.2:n.*83G>A
ENST00000622857.1:c.16-1102G>A ENSP00000481365.1:n.16-1102G>A
NM_175875.4:c.895G>A NP_787071.2:p.Ala299Thr
NM_175875.5:c.895G>A MANE Select NP_787071.3:p.Ala299Thr
Search 100 bp 5'
Search 100 bp 3'