Canonical Allele Identifier: CA679749132
Gene: FADD HGNC NCBI

Linked Data

dbSNP Id: rs1406362446
gnomAD v4: 11-70206077-T-C
MyVariant Identifiers: chr11:g.70052183T>C (hg19) chr11:g.70206077T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.70206077T>C , CM000673.2:g.70206077T>C GRCh38
NC_000011.9:g.70052183T>C , CM000673.1:g.70052183T>C GRCh37
NC_000011.8:g.69729831T>C NCBI36
NG_027966.1:g.7915T>C , LRG_228:g.7915T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000301838.5:c.287-56T>C MANE Select ENSP00000301838.5:n.287-56T>C
ENST00000301838.4:c.287-56T>C ENSP00000301838.4:n.287-56T>C
NM_003824.3:c.287-56T>C , LRG_228t1:c.287-56T>C NP_003815.1:n.287-56T>C
NM_003824.4:c.287-56T>C MANE Select NP_003815.1:n.287-56T>C
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