Canonical Allele Identifier: CA2232921852
Gene: FA2H HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.74713360G= , CM000678.2:g.74713360G= GRCh38
NC_000016.9:g.74747258G= , CM000678.1:g.74747258G= GRCh37
NC_000016.8:g.73304759G= NCBI36
NG_017070.1:g.66472C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000219368.8:c.*830C= MANE Select ENSP00000219368.3:n.*830C=
ENST00000219368.7:c.*830C= ENSP00000219368.3:n.*830C=
ENST00000562145.1:n.1670C=
NM_024306.4:c.*830C= NP_077282.3:n.*830C=
XM_011523319.1:c.*830C= XP_011521621.1:n.*830C=
XM_011523319.2:c.*830C= XP_011521621.1:n.*830C=
NM_024306.5:c.*830C= MANE Select NP_077282.3:n.*830C=
Search 100 bp 5'
Search 100 bp 3'