Canonical Allele Identifier: CA10767534
Gene: FNDC5 HGNC NCBI

Linked Data

dbSNP Id: rs1746661
gnomAD v2: 1-33335039-G-T
gnomAD v3: 1-32869438-G-T
gnomAD v4: 1-32869438-G-T
MyVariant Identifiers: chr1:g.33335039G>T (hg19) chr1:g.32869438G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.32869438G>T , CM000663.2:g.32869438G>T GRCh38
NC_000001.10:g.33335039G>T , CM000663.1:g.33335039G>T GRCh37
NC_000001.9:g.33107626G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000710568.1:c.239-441C>A ENSP00000518350.1:n.239-441C>A
ENST00000373471.9:c.95-441C>A MANE Select ENSP00000362570.5:n.95-441C>A
ENST00000649537.2:c.95-441C>A ENSP00000497837.2:n.95-441C>A
ENST00000373471.7:c.95-441C>A ENSP00000362570.4:n.95-441C>A
ENST00000496770.1:c.-127-445C>A ENSP00000476320.1:n.-127-445C>A
NM_001171940.1:c.95-441C>A NP_001165411.2:n.95-441C>A
NM_001171941.2:c.-127-445C>A NP_001165412.1:n.-127-445C>A
NM_153756.2:c.95-441C>A NP_715637.2:n.95-441C>A
NM_153756.3:c.95-441C>A MANE Select NP_715637.2:n.95-441C>A
NM_001171940.2:c.95-441C>A NP_001165411.2:n.95-441C>A
NM_001171941.3:c.-127-445C>A NP_001165412.1:n.-127-445C>A
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