Canonical Allele Identifier: CA451624766
Gene: RFX6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.117203532A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.116882369A>C , CM000668.2:g.116882369A>C GRCh38
NC_000006.11:g.117203532A>C , CM000668.1:g.117203532A>C GRCh37
NC_000006.10:g.117310225A>C NCBI36
NG_027699.1:g.10157A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000332958.3:c.507A>C MANE Select ENSP00000332208.2:p.Thr169=
ENST00000332958.2:c.507A>C ENSP00000332208.2:p.Thr169=
ENST00000487683.5:n.571A>C
NM_173560.3:c.507A>C NP_775831.2:p.Thr169=
XM_011535589.1:c.507A>C XP_011533891.1:p.Thr169=
XM_017010477.1:c.129A>C XP_016865966.1:p.Thr43=
NM_173560.4:c.507A>C MANE Select NP_775831.2:p.Thr169=
Search 100 bp 5'
Search 100 bp 3'