Canonical Allele Identifier: CA1657429799
Gene: RFX6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.116882317A= , CM000668.2:g.116882317A= GRCh38
NC_000006.11:g.117203480A= , CM000668.1:g.117203480A= GRCh37
NC_000006.10:g.117310173A= NCBI36
NG_027699.1:g.10105A=

Transcript Alleles

HGVS Amino-acid change
ENST00000332958.3:c.505-50A= MANE Select ENSP00000332208.2:n.505-50A=
ENST00000332958.2:c.505-50A= ENSP00000332208.2:n.505-50A=
ENST00000487683.5:n.569-50A=
NM_173560.3:c.505-50A= NP_775831.2:n.505-50A=
XM_011535589.1:c.505-50A= XP_011533891.1:n.505-50A=
XM_017010477.1:c.127-50A= XP_016865966.1:n.127-50A=
NM_173560.4:c.505-50A= MANE Select NP_775831.2:n.505-50A=
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