Canonical Allele Identifier: CA2232922008
Gene: FA2H HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.74713634T= , CM000678.2:g.74713634T= GRCh38
NC_000016.9:g.74747532T= , CM000678.1:g.74747532T= GRCh37
NC_000016.8:g.73305033T= NCBI36
NG_017070.1:g.66198A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000219368.8:c.*556A= MANE Select ENSP00000219368.3:n.*556A=
ENST00000219368.7:c.*556A= ENSP00000219368.3:n.*556A=
ENST00000562145.1:n.1396A=
ENST00000567683.5:c.*954A= ENSP00000455126.1:n.*954A=
NM_024306.4:c.*556A= NP_077282.3:n.*556A=
XM_011523319.1:c.*556A= XP_011521621.1:n.*556A=
XM_011523319.2:c.*556A= XP_011521621.1:n.*556A=
NM_024306.5:c.*556A= MANE Select NP_077282.3:n.*556A=
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Search 100 bp 3'