Canonical Allele Identifier: CA2232921833
Gene: FA2H HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.74713328A= , CM000678.2:g.74713328A= GRCh38
NC_000016.9:g.74747226A= , CM000678.1:g.74747226A= GRCh37
NC_000016.8:g.73304727A= NCBI36
NG_017070.1:g.66504T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000219368.8:c.*862T= MANE Select ENSP00000219368.3:n.*862T=
ENST00000219368.7:c.*862T= ENSP00000219368.3:n.*862T=
ENST00000562145.1:n.1702T=
NM_024306.4:c.*862T= NP_077282.3:n.*862T=
XM_011523319.1:c.*862T= XP_011521621.1:n.*862T=
XM_011523319.2:c.*862T= XP_011521621.1:n.*862T=
NM_024306.5:c.*862T= MANE Select NP_077282.3:n.*862T=
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