Canonical Allele Identifier: CA2713006450
Gene: RFX6 HGNC NCBI

Linked Data

dbSNP Id: rs2114661984
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.116882308G>A , CM000668.2:g.116882308G>A GRCh38
NC_000006.11:g.117203471G>A , CM000668.1:g.117203471G>A GRCh37
NC_000006.10:g.117310164G>A NCBI36
NG_027699.1:g.10096G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000332958.3:c.505-59G>A MANE Select ENSP00000332208.2:n.505-59G>A
ENST00000332958.2:c.505-59G>A ENSP00000332208.2:n.505-59G>A
ENST00000487683.5:n.569-59G>A
NM_173560.3:c.505-59G>A NP_775831.2:n.505-59G>A
XM_011535589.1:c.505-59G>A XP_011533891.1:n.505-59G>A
XM_017010477.1:c.127-59G>A XP_016865966.1:n.127-59G>A
NM_173560.4:c.505-59G>A MANE Select NP_775831.2:n.505-59G>A
Search 100 bp 5'
Search 100 bp 3'