Canonical Allele Identifier: CA2634286401
Gene: FA2H HGNC NCBI

Linked Data

gnomAD v4: 16-74713402-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.74713402G>T , CM000678.2:g.74713402G>T GRCh38
NC_000016.9:g.74747300G>T , CM000678.1:g.74747300G>T GRCh37
NC_000016.8:g.73304801G>T NCBI36
NG_017070.1:g.66430C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000219368.8:c.*788C>A MANE Select ENSP00000219368.3:n.*788C>A
ENST00000219368.7:c.*788C>A ENSP00000219368.3:n.*788C>A
ENST00000562145.1:n.1628C>A
NM_024306.4:c.*788C>A NP_077282.3:n.*788C>A
XM_011523319.1:c.*788C>A XP_011521621.1:n.*788C>A
XM_011523319.2:c.*788C>A XP_011521621.1:n.*788C>A
NM_024306.5:c.*788C>A MANE Select NP_077282.3:n.*788C>A
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