Canonical Allele Identifier: CA365427944
Gene: RFX6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.117203528A>C (hg19) chr6:g.116882365A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.116882365A>C , CM000668.2:g.116882365A>C GRCh38
NC_000006.11:g.117203528A>C , CM000668.1:g.117203528A>C GRCh37
NC_000006.10:g.117310221A>C NCBI36
NG_027699.1:g.10153A>C

Transcript Alleles

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