Canonical Allele Identifier: CA365428131
Gene: RFX6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.116882429G>T , CM000668.2:g.116882429G>T GRCh38
NC_000006.11:g.117203592G>T , CM000668.1:g.117203592G>T GRCh37
NC_000006.10:g.117310285G>T NCBI36
NG_027699.1:g.10217G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000332958.3:c.566+1G>T MANE Select ENSP00000332208.2:n.566+1G>T
ENST00000332958.2:c.566+1G>T ENSP00000332208.2:n.566+1G>T
ENST00000487683.5:n.630+1G>T
NM_173560.3:c.566+1G>T NP_775831.2:n.566+1G>T
XM_011535589.1:c.566+1G>T XP_011533891.1:n.566+1G>T
XM_017010477.1:c.188+1G>T XP_016865966.1:n.188+1G>T
NM_173560.4:c.566+1G>T MANE Select NP_775831.2:n.566+1G>T