Canonical Allele Identifier: CA2387996071

Gene: CHAF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.36414379G= , CM000683.2:g.36414379G=	GRCh38
NC_000021.8:g.37786677G= , CM000683.1:g.37786677G=	GRCh37
NC_000021.7:g.36708547G=	NCBI36
NG_046962.1:g.42323G=

Transcript Alleles

HGVS	Amino-acid Change
NM_005441.3:c.1494-916G= MANE Select	NP_005432.1:n.1494-916G=
ENST00000314103.6:c.1494-916G= MANE Select	ENSP00000315700.4:n.1494-916G=
NM_005441.2:c.1494-916G=	NP_005432.1:n.1494-916G=
ENST00000314103.5:c.1494-916G=	ENSP00000315700.4:n.1494-916G=
XM_011529753.1:c.1494-916G=	XP_011528055.1:n.1494-916G=
XM_011529754.1:c.1494-916G=	XP_011528056.1:n.1494-916G=
XM_011529755.1:c.933-916G=	XP_011528057.1:n.933-916G=
XM_011529755.2:c.933-916G=	XP_011528057.1:n.933-916G=
XM_017028477.1:c.1494-916G=	XP_016883966.1:n.1494-916G=
XM_017028478.1:c.1494-916G=	XP_016883967.1:n.1494-916G=