Canonical Allele Identifier: CA2232921992
Gene: FA2H HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.74713592C= , CM000678.2:g.74713592C= GRCh38
NC_000016.9:g.74747490C= , CM000678.1:g.74747490C= GRCh37
NC_000016.8:g.73304991C= NCBI36
NG_017070.1:g.66240G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000219368.8:c.*598G= MANE Select ENSP00000219368.3:n.*598G=
ENST00000219368.7:c.*598G= ENSP00000219368.3:n.*598G=
ENST00000562145.1:n.1438G=
NM_024306.4:c.*598G= NP_077282.3:n.*598G=
XM_011523319.1:c.*598G= XP_011521621.1:n.*598G=
XM_011523319.2:c.*598G= XP_011521621.1:n.*598G=
NM_024306.5:c.*598G= MANE Select NP_077282.3:n.*598G=
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