Canonical Allele Identifier: CA134809854

Gene: GFOD1

Linked Data

• dbSNP Id: rs567683735
• gnomAD v3: 6-13370298-G-T
• gnomAD v4: 6-13370298-G-T
• MyVariant Identifiers: chr6:g.13370530G>T (hg19) ; chr6:g.13370298G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.13370298G>T , CM000668.2:g.13370298G>T	GRCh38
NC_000006.11:g.13370530G>T , CM000668.1:g.13370530G>T	GRCh37
NC_000006.10:g.13478509G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000379287.4:c.254-4636C>A MANE Select	ENSP00000368589.3:n.254-4636C>A
ENST00000379284.1:c.-56-4636C>A	ENSP00000368586.1:n.-56-4636C>A
ENST00000379287.3:c.254-4636C>A	ENSP00000368589.3:n.254-4636C>A
ENST00000612338.4:c.-56-4636C>A	ENSP00000479493.1:n.-56-4636C>A
NM_001242628.1:c.-56-4636C>A	NP_001229557.1:n.-56-4636C>A
NM_001242630.1:c.-56-4636C>A	NP_001229559.1:n.-56-4636C>A
NM_018988.3:c.254-4636C>A	NP_061861.1:n.254-4636C>A
XM_011514699.1:c.-56-4636C>A	XP_011513001.1:n.-56-4636C>A
XM_011514699.2:c.-56-4636C>A	XP_011513001.1:n.-56-4636C>A
NM_018988.4:c.254-4636C>A MANE Select	NP_061861.1:n.254-4636C>A
NM_001242628.2:c.-56-4636C>A	NP_001229557.1:n.-56-4636C>A
NM_001242630.2:c.-56-4636C>A	NP_001229559.1:n.-56-4636C>A