Canonical Allele Identifier: CA2232982322
Gene: FA2H HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.74774364G= , CM000678.2:g.74774364G= GRCh38
NC_000016.9:g.74808262G= , CM000678.1:g.74808262G= GRCh37
NC_000016.8:g.73365763G= NCBI36
NG_017070.1:g.5468C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000219368.8:c.270+122C= MANE Select ENSP00000219368.3:n.270+122C=
ENST00000219368.7:c.270+122C= ENSP00000219368.3:n.270+122C=
ENST00000567683.5:c.270+122C= ENSP00000455126.1:n.270+122C=
NM_024306.4:c.270+122C= NP_077282.3:n.270+122C=
XM_011523317.1:c.270+122C= XP_011521619.1:n.270+122C=
XM_011523318.1:c.270+122C= XP_011521620.1:n.270+122C=
XM_011523317.3:c.270+122C= XP_011521619.1:n.270+122C=
NM_024306.5:c.270+122C= MANE Select NP_077282.3:n.270+122C=
Search 100 bp 5'
Search 100 bp 3'