Canonical Allele Identifier: CA4364109
Gene: ARPC1B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99391175C>T , CM000669.2:g.99391175C>T GRCh38
NC_000007.13:g.98988798C>T , CM000669.1:g.98988798C>T GRCh37
NC_000007.12:g.98826734C>T NCBI36
NG_055676.1:g.21501C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000414376.6:c.708-3C>T ENSP00000398620.2:n.708-3C>T
ENST00000468337.2:n.1127-3C>T
ENST00000695607.1:n.807-3C>T
ENST00000695608.1:n.1658-3C>T
ENST00000695609.1:n.848C>T
ENST00000417330.6:c.708-3C>T ENSP00000403324.2:n.708-3C>T
ENST00000427217.6:c.708-3C>T ENSP00000403211.2:n.708-3C>T
ENST00000431816.6:c.708-3C>T ENSP00000398110.2:n.708-3C>T
ENST00000443222.6:c.708-3C>T ENSP00000413173.2:n.708-3C>T
ENST00000455009.6:c.708-3C>T ENSP00000410238.2:n.708-3C>T
ENST00000458033.6:c.708-3C>T ENSP00000388802.2:n.708-3C>T
ENST00000638617.1:c.1704-3C>T ENSP00000491073.1:n.1704-3C>T
ENST00000645391.1:c.708-3C>T ENSP00000494033.1:n.708-3C>T
ENST00000646101.2:c.708-3C>T MANE Select ENSP00000496599.1:n.708-3C>T
ENST00000252725.9:c.708-3C>T ENSP00000252725.5:n.708-3C>T
ENST00000451682.5:c.708-3C>T ENSP00000389631.1:n.708-3C>T
ENST00000481997.5:n.229-3C>T
NM_005720.3:c.708-3C>T NP_005711.1:n.708-3C>T
XM_006715825.1:c.708-3C>T XP_006715888.1:n.708-3C>T
XM_006715826.1:c.708-3C>T XP_006715889.1:n.708-3C>T
NM_005720.4:c.708-3C>T MANE Select NP_005711.1:n.708-3C>T
XM_006715825.2:c.708-3C>T XP_006715888.1:n.708-3C>T
XM_006715826.2:c.708-3C>T XP_006715889.1:n.708-3C>T
XM_024446628.1:c.708-3C>T XP_024302396.1:n.708-3C>T
XM_024446629.1:c.708-3C>T XP_024302397.1:n.708-3C>T
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