Canonical Allele Identifier: CA463549376
Gene: FBXL6 HGNC NCBI
SLC52A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.145581856C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.144358196C>G , CM000670.2:g.144358196C>G GRCh38
NC_000008.10:g.145581856C>G , CM000670.1:g.145581856C>G GRCh37
NC_000008.9:g.145552664C>G NCBI36
NG_032872.1:g.4640C>G
NG_032872.2:g.4640C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000331890.6:c.252G>C (FBXL6) MANE Select ENSP00000330098.5:p.Gly84=
ENST00000532815.2:c.-111+594C>G (SLC52A2) ENSP00000501933.1:n.-111+594C>G
ENST00000675292.1:c.-110-988C>G (SLC52A2) ENSP00000502652.1:n.-110-988C>G
ENST00000675888.1:c.-110-988C>G (SLC52A2) ENSP00000502294.1:n.-110-988C>G
ENST00000331890.5:c.252G>C (FBXL6) ENSP00000330098.5:p.Gly84=
ENST00000455319.6:c.252G>C (FBXL6) ENSP00000403873.2:p.Gly84=
ENST00000524541.5:c.-110-988C>G (SLC52A2) ENSP00000434239.1:n.-110-988C>G
ENST00000530142.5:n.1078G>C (FBXL6)
ENST00000532815.1:n.399+594C>G (SLC52A2)
NM_012162.3:c.252G>C (FBXL6) NP_036294.2:p.Gly84=
NM_024555.5:c.252G>C (FBXL6) NP_078831.4:p.Gly84=
NM_012162.4:c.252G>C (FBXL6) MANE Select NP_036294.2:p.Gly84=
NM_024555.6:c.252G>C (FBXL6) NP_078831.4:p.Gly84=