Canonical Allele Identifier: CA381665954
Gene: FADD HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.70052278G>T (hg19) chr11:g.70206172G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.70206172G>T , CM000673.2:g.70206172G>T GRCh38
NC_000011.9:g.70052278G>T , CM000673.1:g.70052278G>T GRCh37
NC_000011.8:g.69729926G>T NCBI36
NG_027966.1:g.8010G>T , LRG_228:g.8010G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000301838.5:c.326G>T MANE Select ENSP00000301838.5:p.Gly109Val
ENST00000301838.4:c.326G>T ENSP00000301838.4:p.Gly109Val
NM_003824.3:c.326G>T , LRG_228t1:c.326G>T NP_003815.1:p.Gly109Val
NM_003824.4:c.326G>T MANE Select NP_003815.1:p.Gly109Val
Search 100 bp 5'
Search 100 bp 3'