Canonical Allele Identifier: CA2232921868

Gene: FA2H

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.74713385G= , CM000678.2:g.74713385G=	GRCh38
NC_000016.9:g.74747283G= , CM000678.1:g.74747283G=	GRCh37
NC_000016.8:g.73304784G=	NCBI36
NG_017070.1:g.66447C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219368.8:c.*805C= MANE Select	ENSP00000219368.3:n.*805C=
ENST00000219368.7:c.*805C=	ENSP00000219368.3:n.*805C=
ENST00000562145.1:n.1645C=
NM_024306.4:c.*805C=	NP_077282.3:n.*805C=
XM_011523319.1:c.*805C=	XP_011521621.1:n.*805C=
XM_011523319.2:c.*805C=	XP_011521621.1:n.*805C=
NM_024306.5:c.*805C= MANE Select	NP_077282.3:n.*805C=