Canonical Allele Identifier: CA2737526574
Gene: CHAF1B HGNC NCBI

Linked Data

dbSNP Id: rs2835342
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Genomic Alleles

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

Transcript Alleles

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