Canonical Allele Identifier: CA1441689256
Gene: FAM184B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.17681242T= , CM000666.2:g.17681242T= GRCh38
NC_000004.11:g.17682865T= , CM000666.1:g.17682865T= GRCh37
NC_000004.10:g.17291963T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265018.4:c.1596+7182A= MANE Select ENSP00000265018.3:n.1596+7182A=
ENST00000265018.3:c.1596+7182A= ENSP00000265018.3:n.1596+7182A=
NM_015688.1:c.1596+7182A= NP_056503.1:n.1596+7182A=
XM_011513834.1:c.1596+7182A= XP_011512136.1:n.1596+7182A=
NM_015688.2:c.1596+7182A= MANE Select NP_056503.1:n.1596+7182A=