Canonical Allele Identifier: CA2232921884

Gene: FA2H

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.74713411C= , CM000678.2:g.74713411C=	GRCh38
NC_000016.9:g.74747309C= , CM000678.1:g.74747309C=	GRCh37
NC_000016.8:g.73304810C=	NCBI36
NG_017070.1:g.66421G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219368.8:c.*779G= MANE Select	ENSP00000219368.3:n.*779G=
ENST00000219368.7:c.*779G=	ENSP00000219368.3:n.*779G=
ENST00000562145.1:n.1619G=
NM_024306.4:c.*779G=	NP_077282.3:n.*779G=
XM_011523319.1:c.*779G=	XP_011521621.1:n.*779G=
XM_011523319.2:c.*779G=	XP_011521621.1:n.*779G=
NM_024306.5:c.*779G= MANE Select	NP_077282.3:n.*779G=