Canonical Allele Identifier: CA14897696

Gene: CHAF1B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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