Canonical Allele Identifier: CA2634286154
Gene: FA2H HGNC NCBI

Linked Data

gnomAD v4: 16-74713313-GT-G
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.74713317del , CM000678.2:g.74713317del GRCh38
NC_000016.9:g.74747215del , CM000678.1:g.74747215del GRCh37
NC_000016.8:g.73304716del NCBI36
NG_017070.1:g.66518del

Transcript Alleles

HGVS Amino-acid Change
ENST00000219368.8:c.*876del MANE Select ENSP00000219368.3:n.*876del
ENST00000219368.7:c.*876del ENSP00000219368.3:n.*876del
ENST00000562145.1:n.1716del
NM_024306.4:c.*876del NP_077282.3:n.*876del
XM_011523319.1:c.*876del XP_011521621.1:n.*876del
XM_011523319.2:c.*876del XP_011521621.1:n.*876del
NM_024306.5:c.*876del MANE Select NP_077282.3:n.*876del
Search 100 bp 5'
Search 100 bp 3'